"Ambry Genetics"[submitter] AND "KCNK10"[gene] - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2489140	NM_138317.3(KCNK10):c.1591C>T (p.Arg531Trp)	KCNK10 (R531W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376416	NM_138317.3(KCNK10):c.1498A>G (p.Asn500Asp)	KCNK10 (N495D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322629	NM_138317.3(KCNK10):c.1472A>C (p.Lys491Thr)	KCNK10 (K491T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315764	NM_138317.3(KCNK10):c.1462G>A (p.Glu488Lys)	KCNK10 (E488K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274570	NM_138317.3(KCNK10):c.1445G>A (p.Arg482Gln)	KCNK10 (R482Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3113357	NM_138317.3(KCNK10):c.1444C>T (p.Arg482Trp)	KCNK10 (R477W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286832	NM_138317.3(KCNK10):c.1439C>T (p.Thr480Ile)	KCNK10 (T475I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2369108	NM_138317.3(KCNK10):c.1315C>T (p.His439Tyr)	KCNK10 (H439Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3113356	NM_138317.3(KCNK10):c.1234C>T (p.Arg412Cys)	KCNK10 (R407C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370428	NM_138317.3(KCNK10):c.1231G>A (p.Gly411Ser)	KCNK10 (G406S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464925	NM_138317.3(KCNK10):c.1147C>T (p.Arg383Trp)	KCNK10 (R378W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532704	NM_138317.3(KCNK10):c.1133G>A (p.Arg378His)	KCNK10 (R378H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3113355	NM_138317.3(KCNK10):c.1132C>T (p.Arg378Cys)	KCNK10 (R378C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3113354	NM_138317.3(KCNK10):c.1117C>T (p.Arg373Trp)	KCNK10 (R368W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3113353	NM_138317.3(KCNK10):c.1107T>A (p.Asp369Glu)	KCNK10 (D364E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297135	NM_138317.3(KCNK10):c.1049C>T (p.Ala350Val)	KCNK10 (A350V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345054	NM_138317.3(KCNK10):c.897G>C (p.Glu299Asp)	KCNK10 (E299D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216857	NM_138317.3(KCNK10):c.877G>T (p.Ala293Ser)	KCNK10 (A293S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3113359	NM_138317.3(KCNK10):c.651A>T (p.Lys217Asn)	KCNK10 (K217N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623652	NM_138317.3(KCNK10):c.556A>G (p.Lys186Glu)	KCNK10 (K181E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539595	NM_138317.3(KCNK10):c.377C>T (p.Pro126Leu)	KCNK10 (P121L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490385	NM_138317.3(KCNK10):c.355C>T (p.Arg119Trp)	KCNK10 (R119W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464883	NM_138317.3(KCNK10):c.344C>T (p.Ala115Val)	KCNK10 (A115V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3113358	NM_138317.3(KCNK10):c.293T>C (p.Leu98Ser)	KCNK10 (L98S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491553	NM_138317.3(KCNK10):c.286C>T (p.Arg96Trp)	KCNK10 (R91W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357815	NM_138317.3(KCNK10):c.232G>C (p.Val78Leu)	KCNK10 (V73L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517330	NM_138317.3(KCNK10):c.140G>A (p.Arg47His)	KCNK10 (R47H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511015	NM_138317.3(KCNK10):c.139C>T (p.Arg47Cys)	KCNK10 (R42C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2602812	NM_138317.3(KCNK10):c.119C>T (p.Pro40Leu)	KCNK10 (P35L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268471	NM_138317.3(KCNK10):c.92G>A (p.Ser31Asn)	KCNK10 (S26N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511574	NM_138317.3(KCNK10):c.64G>A (p.Ala22Thr)	KCNK10 (A22T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 31