"Ambry Genetics"[submitter] AND "KLRG2"[gene] - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3289110	NM_198508.4(KLRG2):c.1177G>A (p.Ala393Thr)	KLRG2 (A393T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115941	NM_198508.4(KLRG2):c.1171C>G (p.Leu391Val)	KLRG2 (L391V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115940	NM_198508.4(KLRG2):c.1148G>A (p.Cys383Tyr)	KLRG2 (C383Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345711	NM_198508.4(KLRG2):c.1123G>A (p.Gly375Ser)	KLRG2 (G375S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247019	NM_198508.4(KLRG2):c.1093C>T (p.Pro365Ser)	KLRG2 (P365S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115938	NM_198508.4(KLRG2):c.1037A>G (p.His346Arg)	KLRG2 (H346R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115948	NM_198508.4(KLRG2):c.976G>A (p.Ala326Thr)	KLRG2 (A326T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115947	NM_198508.4(KLRG2):c.937G>T (p.Ala313Ser)	KLRG2 (A313S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209588	NM_198508.4(KLRG2):c.901G>A (p.Glu301Lys)	KLRG2 (E301K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382292	NM_198508.4(KLRG2):c.838G>T (p.Val280Leu)	KLRG2 (V280L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115946	NM_198508.4(KLRG2):c.818C>A (p.Ala273Glu)	KLRG2 (A273E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2568432	NM_198508.4(KLRG2):c.763C>T (p.Pro255Ser)	KLRG2 (P255S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289112	NM_198508.4(KLRG2):c.641G>C (p.Gly214Ala)	KLRG2 (G214A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115945	NM_198508.4(KLRG2):c.605G>T (p.Arg202Leu)	KLRG2 (R202L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377314	NM_198508.4(KLRG2):c.574C>G (p.Arg192Gly)	KLRG2, LOC129999472 (R192G)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3115943	NM_198508.4(KLRG2):c.514C>A (p.Leu172Met)	KLRG2, LOC129999472 (L172M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333078	NM_198508.4(KLRG2):c.512T>A (p.Leu171His)	KLRG2, LOC129999472 (L171H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379479	NM_198508.4(KLRG2):c.475C>T (p.Pro159Ser)	KLRG2, LOC129999472 (P159S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255440	NM_198508.4(KLRG2):c.445C>G (p.Arg149Gly)	KLRG2, LOC129999472 (R149G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461685	NM_198508.4(KLRG2):c.382G>A (p.Val128Met)	KLRG2, LOC129999472 (V128M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392463	NM_198508.4(KLRG2):c.322G>A (p.Glu108Lys)	KLRG2, LOC129999472 (E108K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289111	NM_198508.4(KLRG2):c.265G>T (p.Val89Phe)	KLRG2 (V89F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491047	NM_198508.4(KLRG2):c.265G>A (p.Val89Ile)	KLRG2 (V89I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305936	NM_198508.4(KLRG2):c.173C>T (p.Ala58Val)	KLRG2 (A58V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467351	NM_198508.4(KLRG2):c.165G>C (p.Glu55Asp)	KLRG2 (E55D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407746	NM_198508.4(KLRG2):c.158C>T (p.Ala53Val)	KLRG2 (A53V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115939	NM_198508.4(KLRG2):c.103C>A (p.Pro35Thr)	KLRG2 (P35T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295939	NM_198508.4(KLRG2):c.76G>C (p.Val26Leu)	KLRG2 (V26L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269915	NM_198508.4(KLRG2):c.67G>A (p.Gly23Arg)	KLRG2 (G23R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115942	NM_198508.4(KLRG2):c.15G>T (p.Trp5Cys)	KLRG2 (W5C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482953	NM_198508.4(KLRG2):c.10T>G (p.Ser4Ala)	KLRG2 (S4A)	Single nucleotide variant (missense variant)	not specified	GLikely benign

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Items: 31