KCNJ15[gene] and "single gene"[properties] - ClinVar

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Items: 29

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3113326	NM_170736.3(KCNJ15):c.4G>T (p.Asp2Tyr)	KCNJ15 (D2Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234329	NM_170736.3(KCNJ15):c.8C>T (p.Ala3Val)	KCNJ15 (A3V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623600	NM_170736.3(KCNJ15):c.10A>T (p.Ile4Phe)	KCNJ15 (I4F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 770817	NM_170736.3(KCNJ15):c.16A>G (p.Ile6Val)	KCNJ15 (I6V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3113324	NM_170736.3(KCNJ15):c.19G>A (p.Gly7Ser)	KCNJ15 (G7S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2293160	NM_170736.3(KCNJ15):c.29G>A (p.Ser10Asn)	KCNJ15 (S10N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3287642	NM_170736.3(KCNJ15):c.62G>T (p.Gly21Val)	KCNJ15 (G21V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3287646	NM_170736.3(KCNJ15):c.68A>G (p.Lys23Arg)	KCNJ15 (K23R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212571	NM_170736.3(KCNJ15):c.73A>T (p.Asn25Tyr)	KCNJ15 (N25Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603005	NM_170736.3(KCNJ15):c.122A>G (p.Asp41Gly)	KCNJ15 (D41G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3113325	NM_170736.3(KCNJ15):c.311A>G (p.His104Arg)	KCNJ15 (H104R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486413	NM_170736.3(KCNJ15):c.421C>T (p.His141Tyr)	KCNJ15 (H141Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3287643	NM_170736.3(KCNJ15):c.505G>A (p.Ala169Thr)	KCNJ15 (A169T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3113327	NM_170736.3(KCNJ15):c.521G>A (p.Arg174Gln)	KCNJ15 (R174Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2488312	NM_170736.3(KCNJ15):c.601A>G (p.Asn201Asp)	KCNJ15 (N201D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3113328	NM_170736.3(KCNJ15):c.616C>T (p.Leu206Phe)	KCNJ15 (L206F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3113329	NM_170736.3(KCNJ15):c.660C>G (p.His220Gln)	KCNJ15 (H220Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3113330	NM_170736.3(KCNJ15):c.679C>T (p.Arg227Trp)	KCNJ15 (R227W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2560031	NM_170736.3(KCNJ15):c.805C>A (p.Pro269Thr)	KCNJ15 (P269T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3287644	NM_170736.3(KCNJ15):c.851A>G (p.Asn284Ser)	KCNJ15 (N284S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3113331	NM_170736.3(KCNJ15):c.949C>G (p.Leu317Val)	KCNJ15 (L317V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3113332	NM_170736.3(KCNJ15):c.991G>A (p.Glu331Lys)	KCNJ15 (E331K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215204	NM_170736.3(KCNJ15):c.1010C>A (p.Pro337Gln)	KCNJ15 (P337Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3287645	NM_170736.3(KCNJ15):c.1016G>T (p.Cys339Phe)	KCNJ15 (C339F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238653	NM_170736.3(KCNJ15):c.1027T>C (p.Cys343Arg)	KCNJ15 (C343R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3113323	NM_170736.3(KCNJ15):c.1029T>G (p.Cys343Trp)	KCNJ15 (C343W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542689	NM_170736.3(KCNJ15):c.1036T>A (p.Ser346Thr)	KCNJ15 (S346T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 816167	GRCh37/hg19 21q22.13(chr21:39602066-39667589)x1	KCNJ15	Copy number loss	not provided	GUncertain significance
Select item 564646	GRCh37/hg19 21q22.13(chr21:39593444-39646635)x1	KCNJ15	Copy number loss	not provided	GUncertain significance

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Items: 29