Related gene-specific medical variations for Gene (Select 25999) - ClinVar

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Items: 37

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3267769	NM_015526.3(CLIP3):c.796G>A (p.Val266Met)	CLIP3, LOC101927572 (V266M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3267768	NM_015526.3(CLIP3):c.445C>A (p.Leu149Met)	CLIP3, LOC101927572 (L149M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3267767	NM_015526.3(CLIP3):c.1415G>C (p.Arg472Thr)	CLIP3, LOC101927572 (R472T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3267765	NM_015526.3(CLIP3):c.821A>G (p.Lys274Arg)	CLIP3, LOC101927572 (K274R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145854	NM_015526.3(CLIP3):c.88G>T (p.Ala30Ser)	CLIP3, LOC101927572 (A30S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145853	NM_015526.3(CLIP3):c.847G>A (p.Val283Ile)	CLIP3, LOC101927572 (V283I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145852	NM_015526.3(CLIP3):c.79G>A (p.Val27Ile)	CLIP3, LOC101927572 (V27I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145851	NM_015526.3(CLIP3):c.775C>T (p.Arg259Trp)	CLIP3, LOC101927572 (R259W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145850	NM_015526.3(CLIP3):c.686G>A (p.Arg229Gln)	CLIP3, LOC101927572 (R229Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145849	NM_015526.3(CLIP3):c.314G>A (p.Arg105His)	CLIP3, LOC101927572 (R105H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145847	NM_015526.3(CLIP3):c.1237G>A (p.Gly413Arg)	CLIP3, LOC101927572 (G413R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3145846	NM_015526.3(CLIP3):c.1166G>C (p.Gly389Ala)	CLIP3, LOC101927572 (G389A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2624260	NM_015526.3(CLIP3):c.279G>C (p.Gln93His)	CLIP3, LOC101927572 (Q93H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620692	NM_015526.3(CLIP3):c.557C>A (p.Pro186Gln)	CLIP3, LOC101927572 (P186Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596765	NM_015526.3(CLIP3):c.674C>T (p.Ala225Val)	CLIP3, LOC101927572 (A225V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588345	NM_015526.3(CLIP3):c.1150C>T (p.Arg384Cys)	CLIP3, LOC101927572 (R384C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542766	NM_015526.3(CLIP3):c.1143C>G (p.Asp381Glu)	CLIP3, LOC101927572 (D381E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516344	NM_015526.3(CLIP3):c.1486G>A (p.Val496Ile)	CLIP3, LOC101927572 (V496I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508606	NM_015526.3(CLIP3):c.1532G>A (p.Arg511His)	CLIP3, LOC101927572 (R511H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508059	NM_015526.3(CLIP3):c.1232G>A (p.Arg411His)	CLIP3, LOC101927572 (R411H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470797	NM_015526.3(CLIP3):c.533G>A (p.Arg178His)	CLIP3, LOC101927572 (R178H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393127	NM_015526.3(CLIP3):c.410C>T (p.Ala137Val)	CLIP3, LOC101927572 (A137V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389819	NM_015526.3(CLIP3):c.779C>T (p.Thr260Met)	CLIP3, LOC101927572 (T260M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389783	NM_015526.3(CLIP3):c.811G>A (p.Ala271Thr)	CLIP3, LOC101927572 (A271T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349359	NM_015526.3(CLIP3):c.1169G>A (p.Arg390His)	CLIP3, LOC101927572 (R390H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346261	NM_015526.3(CLIP3):c.1477G>A (p.Gly493Arg)	CLIP3, LOC101927572 (G493R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335338	NM_015526.3(CLIP3):c.187A>C (p.Asn63His)	CLIP3, LOC101927572 (N63H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324641	NM_015526.3(CLIP3):c.1052A>G (p.Gln351Arg)	CLIP3, LOC101927572 (Q351R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310675	NM_015526.3(CLIP3):c.1306G>A (p.Gly436Arg)	CLIP3, LOC101927572 (G436R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302928	NM_015526.3(CLIP3):c.565G>A (p.Val189Met)	CLIP3, LOC101927572 (V189M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290424	NM_015526.3(CLIP3):c.862A>C (p.Met288Leu)	CLIP3, LOC101927572 (M288L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268842	NM_015526.3(CLIP3):c.1159G>A (p.Gly387Ser)	CLIP3, LOC101927572 (G387S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251204	NM_015526.3(CLIP3):c.1298G>A (p.Arg433His)	CLIP3, LOC101927572 (R433H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235449	NM_015526.3(CLIP3):c.94A>C (p.Ser32Arg)	CLIP3, LOC101927572 (S32R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228316	NM_015526.3(CLIP3):c.443C>T (p.Ala148Val)	CLIP3, LOC101927572 (A148V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2223345	NM_015526.3(CLIP3):c.752C>T (p.Ala251Val)	CLIP3, LOC101927572 (A251V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208955	NM_015526.3(CLIP3):c.884G>A (p.Arg295His)	CLIP3, LOC101927572 (R295H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Links from Gene

Items: 37