KIFC1[gene] and "single gene"[properties] - ClinVar

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Items: 45

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2556947	NM_002263.4(KIFC1):c.19C>T (p.Pro7Ser)	KIFC1 (P7S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399688	NM_002263.4(KIFC1):c.44T>C (p.Ile15Thr)	KIFC1 (I15T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2247357	NM_002263.4(KIFC1):c.70G>T (p.Ala24Ser)	KIFC1 (A24S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115027	NM_002263.4(KIFC1):c.114G>T (p.Arg38Ser)	KIFC1 (R38S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300382	NM_002263.4(KIFC1):c.154C>T (p.Arg52Trp)	KIFC1 (R52W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243405	NM_002263.4(KIFC1):c.274G>C (p.Gly92Arg)	KIFC1 (G92R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288681	NM_002263.4(KIFC1):c.281G>A (p.Arg94Gln)	KIFC1 (R94Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207038	NM_002263.4(KIFC1):c.448C>G (p.Leu150Val)	KIFC1 (L150V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115039	NM_002263.4(KIFC1):c.716A>T (p.Glu239Val)	KIFC1 (E239V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487295	NM_002263.4(KIFC1):c.722G>A (p.Arg241Gln)	KIFC1 (R241Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272770	NM_002263.4(KIFC1):c.728G>T (p.Gly243Val)	KIFC1 (G243V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115040	NM_002263.4(KIFC1):c.779C>T (p.Ala260Val)	KIFC1 (A260V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522281	NM_002263.4(KIFC1):c.841G>A (p.Ala281Thr)	KIFC1 (A281T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2602026	NM_002263.4(KIFC1):c.856C>T (p.Arg286Trp)	KIFC1 (R286W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248568	NM_002263.4(KIFC1):c.866G>A (p.Arg289His)	KIFC1 (R289H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317058	NM_002263.4(KIFC1):c.965C>T (p.Pro322Leu)	KIFC1 (P322L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334489	NM_002263.4(KIFC1):c.994C>T (p.Leu332Phe)	KIFC1 (L332F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2479519	NM_002263.4(KIFC1):c.1040G>A (p.Arg347His)	KIFC1 (R347H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2600055	NM_002263.4(KIFC1):c.1066C>T (p.Arg356Trp)	KIFC1 (R356W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548437	NM_002263.4(KIFC1):c.1082G>T (p.Ser361Ile)	KIFC1 (S361I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482194	NM_002263.4(KIFC1):c.1096C>A (p.Pro366Thr)	KIFC1 (P366T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535817	NM_002263.4(KIFC1):c.1102A>G (p.Thr368Ala)	KIFC1 (T368A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115025	NM_002263.4(KIFC1):c.1121T>G (p.Phe374Cys)	KIFC1 (F374C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548603	NM_002263.4(KIFC1):c.1134C>G (p.Phe378Leu)	KIFC1 (F378L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115026	NM_002263.4(KIFC1):c.1138C>T (p.Pro380Ser)	KIFC1 (P380S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390438	NM_002263.4(KIFC1):c.1328C>G (p.Ser443Cys)	KIFC1 (S443C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115029	NM_002263.4(KIFC1):c.1366A>C (p.Ser456Arg)	KIFC1 (S456R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344396	NM_002263.4(KIFC1):c.1385T>C (p.Val462Ala)	KIFC1 (V462A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288683	NM_002263.4(KIFC1):c.1438G>C (p.Gly480Arg)	KIFC1 (G480R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115030	NM_002263.4(KIFC1):c.1466G>A (p.Arg489His)	KIFC1 (R489H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2272975	NM_002263.4(KIFC1):c.1493C>T (p.Thr498Ile)	KIFC1 (T498I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2604068	NM_002263.4(KIFC1):c.1541A>G (p.Asp514Gly)	KIFC1 (D514G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115031	NM_002263.4(KIFC1):c.1562G>A (p.Arg521His)	KIFC1 (R521H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3115032	NM_002263.4(KIFC1):c.1601G>A (p.Arg534Gln)	KIFC1 (R534Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115033	NM_002263.4(KIFC1):c.1658G>A (p.Arg553Gln)	KIFC1 (R553Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115034	NM_002263.4(KIFC1):c.1669T>G (p.Cys557Gly)	KIFC1 (C557G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521715	NM_002263.4(KIFC1):c.1669T>C (p.Cys557Arg)	KIFC1 (C557R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341331	NM_002263.4(KIFC1):c.1735G>A (p.Gly579Ser)	KIFC1 (G579S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3288682	NM_002263.4(KIFC1):c.1741G>A (p.Gly581Arg)	KIFC1 (G581R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115035	NM_002263.4(KIFC1):c.1748G>T (p.Arg583Leu)	KIFC1 (R583L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115036	NM_002263.4(KIFC1):c.1778A>T (p.Asn593Ile)	KIFC1 (N593I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507662	NM_002263.4(KIFC1):c.1846C>T (p.Arg616Trp)	KIFC1 (R616W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115037	NM_002263.4(KIFC1):c.1931A>G (p.Glu644Gly)	KIFC1 (E644G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3115038	NM_002263.4(KIFC1):c.2011A>C (p.Asn671His)	KIFC1 (N671H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 403017	NM_002263.4(KIFC1):c.15_16dup	KIFC1	Insertion (3 prime UTR variant)	not specified	GBenign

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Items: 45