KCNA10[gene] and "single gene"[properties] - ClinVar

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Items: 40

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2322793	NM_005549.2(KCNA10):c.1439T>C (p.Ile480Thr)	KCNA10 (I480T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620548	NM_005549.2(KCNA10):c.1307T>C (p.Ile436Thr)	KCNA10 (I436T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204528	NM_005549.2(KCNA10):c.1298G>T (p.Gly433Val)	KCNA10 (G433V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3113009	NM_005549.2(KCNA10):c.1288A>G (p.Thr430Ala)	KCNA10 (T430A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268118	NM_005549.2(KCNA10):c.1261A>G (p.Thr421Ala)	KCNA10 (T421A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2493857	NM_005549.2(KCNA10):c.1250T>C (p.Val417Ala)	KCNA10 (V417A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243565	NM_005549.2(KCNA10):c.1150A>G (p.Ile384Val)	KCNA10 (I384V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 787752	NM_005549.2(KCNA10):c.1118G>A (p.Arg373Gln)	KCNA10 (R373Q)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 769523	NM_005549.2(KCNA10):c.1089C>A (p.Ile363=)	KCNA10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3113007	NM_005549.2(KCNA10):c.1060C>T (p.Leu354Phe)	KCNA10 (L354F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617921	NM_005549.2(KCNA10):c.962C>T (p.Thr321Ile)	KCNA10 (T321I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3287483	NM_005549.2(KCNA10):c.865C>T (p.Arg289Trp)	KCNA10 (R289W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3287487	NM_005549.2(KCNA10):c.844T>C (p.Phe282Leu)	KCNA10 (F282L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3113017	NM_005549.2(KCNA10):c.838G>T (p.Val280Leu)	KCNA10 (V280L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3113016	NM_005549.2(KCNA10):c.784C>G (p.Leu262Val)	KCNA10 (L262V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3287485	NM_005549.2(KCNA10):c.779C>T (p.Thr260Ile)	KCNA10 (T260I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 775575	NM_005549.2(KCNA10):c.761A>G (p.Asn254Ser)	KCNA10 (N254S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2608422	NM_005549.2(KCNA10):c.757C>T (p.Pro253Ser)	KCNA10 (P253S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3287486	NM_005549.2(KCNA10):c.743A>G (p.Lys248Arg)	KCNA10 (K248R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226552	NM_005549.2(KCNA10):c.724C>T (p.Arg242Trp)	KCNA10 (R242W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3113015	NM_005549.2(KCNA10):c.720G>T (p.Glu240Asp)	KCNA10 (E240D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285106	NM_005549.2(KCNA10):c.695T>G (p.Ile232Ser)	KCNA10 (I232S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3358893	NM_005549.2(KCNA10):c.682A>G (p.Ile228Val)	KCNA10 (I228V)	Single nucleotide variant (missense variant)	Congenital long QT syndrome	GUncertain significance
Select item 2250695	NM_005549.2(KCNA10):c.674T>C (p.Val225Ala)	KCNA10 (V225A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 787753	NM_005549.2(KCNA10):c.666G>A (p.Ser222=)	KCNA10	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2618639	NM_005549.2(KCNA10):c.665C>T (p.Ser222Leu)	KCNA10 (S222L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1294562	NM_005549.2(KCNA10):c.658G>A (p.Val220Met)	KCNA10 (V220M)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3113014	NM_005549.2(KCNA10):c.608G>T (p.Trp203Leu)	KCNA10 (W203L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559795	NM_005549.2(KCNA10):c.599G>T (p.Arg200Leu)	KCNA10 (R200L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3113013	NM_005549.2(KCNA10):c.524C>A (p.Ala175Asp)	KCNA10 (A175D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533059	NM_005549.2(KCNA10):c.499T>C (p.Ser167Pro)	KCNA10 (S167P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213091	NM_005549.2(KCNA10):c.404G>A (p.Arg135Gln)	KCNA10 (R135Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3113012	NM_005549.2(KCNA10):c.403C>G (p.Arg135Gly)	KCNA10 (R135G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338648	NM_005549.2(KCNA10):c.375G>A (p.Met125Ile)	KCNA10 (M125I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3113011	NM_005549.2(KCNA10):c.343C>T (p.Arg115Trp)	KCNA10 (R115W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3113010	NM_005549.2(KCNA10):c.320T>A (p.Phe107Tyr)	KCNA10 (F107Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489139	NM_005549.2(KCNA10):c.236T>G (p.Val79Gly)	KCNA10 (V79G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2394753	NM_005549.2(KCNA10):c.216C>G (p.Asp72Glu)	KCNA10 (D72E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3113008	NM_005549.2(KCNA10):c.119G>A (p.Arg40Gln)	KCNA10 (R40Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3287484	NM_005549.2(KCNA10):c.104C>T (p.Thr35Ile)	KCNA10 (T35I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 40