SMIM15[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2609470	NM_001048249.4(SMIM15):c.194T>C (p.Ile65Thr)	SMIM15 (I65T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2523958	NM_001048249.4(SMIM15):c.182G>A (p.Arg61His)	SMIM15 (R61H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337588	NM_001048249.4(SMIM15):c.172A>C (p.Lys58Gln)	SMIM15 (K58Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320973	NM_001048249.4(SMIM15):c.136A>G (p.Lys46Glu)	SMIM15 (K46E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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