Related gene-specific medical variations for Gene (Select 146223) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3146259	NM_181553.4(CMTM3):c.82C>T (p.Arg28Cys)	CMTM3, CMTM4 +1 more (R28C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3146258	NM_181553.4(CMTM3):c.40C>A (p.Pro14Thr)	CMTM3, CMTM4 +1 more (P14T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2613899	NM_181553.4(CMTM3):c.371A>G (p.Tyr124Cys)	CMTM3, CMTM4 (Y124C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2597350	NM_181553.4(CMTM3):c.85G>A (p.Ala29Thr)	CMTM3, CMTM4 +1 more (A29T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2372808	NM_181553.4(CMTM3):c.422T>C (p.Ile141Thr)	CMTM3, CMTM4 (I141T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2302902	NM_181553.4(CMTM3):c.182C>T (p.Ala61Val)	CMTM3, CMTM4 (A61V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2233201	NM_181553.4(CMTM3):c.352A>G (p.Ile118Val)	CMTM3, CMTM4 (I118V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar