Related gene-specific medical variations for Gene (Select 79733) - ClinVar

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Items: 41

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2621287	NM_024680.4(E2F8):c.2298G>C (p.Glu766Asp)	CSRP3-AS1, E2F8 (E766D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2588636	NM_024680.4(E2F8):c.1084C>G (p.His362Asp)	CSRP3-AS1, E2F8 (H362D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2556801	NM_024680.4(E2F8):c.133C>T (p.Pro45Ser)	CSRP3-AS1, E2F8 (P45S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2553215	NM_024680.4(E2F8):c.749G>A (p.Gly250Glu)	CSRP3-AS1, E2F8 (G250E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2545208	NM_024680.4(E2F8):c.2474G>A (p.Arg825His)	CSRP3-AS1, E2F8 (R825H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2542244	NM_024680.4(E2F8):c.2306A>G (p.Asn769Ser)	CSRP3-AS1, E2F8 (N769S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2539989	NM_024680.4(E2F8):c.2183A>T (p.Asn728Ile)	CSRP3-AS1, E2F8 (N728I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2520430	NM_024680.4(E2F8):c.635A>G (p.Lys212Arg)	CSRP3-AS1, E2F8 (K212R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2517087	NM_024680.4(E2F8):c.1490T>A (p.Val497Asp)	CSRP3-AS1, E2F8 (V497D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2491550	NM_024680.4(E2F8):c.1063A>G (p.Ser355Gly)	E2F8, CSRP3-AS1 (S355G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2479659	NM_024680.4(E2F8):c.1400G>A (p.Gly467Glu)	CSRP3-AS1, E2F8 (G467E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2471101	NM_024680.4(E2F8):c.1460C>T (p.Ala487Val)	CSRP3-AS1, E2F8 (A487V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2469579	NM_024680.4(E2F8):c.2240A>G (p.Asn747Ser)	CSRP3-AS1, E2F8 (N747S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2399288	NM_024680.4(E2F8):c.1963T>C (p.Ser655Pro)	CSRP3-AS1, E2F8 (S655P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2381951	NM_024680.4(E2F8):c.1642C>T (p.His548Tyr)	CSRP3-AS1, E2F8 (H548Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2379300	NM_024680.4(E2F8):c.2281G>A (p.Val761Met)	E2F8, CSRP3-AS1 (V761M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2365966	NM_024680.4(E2F8):c.884T>C (p.Ile295Thr)	CSRP3-AS1, E2F8 (I295T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2359220	NM_024680.4(E2F8):c.751G>A (p.Val251Met)	CSRP3-AS1, E2F8 (V251M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2357049	NM_024680.4(E2F8):c.1999C>G (p.His667Asp)	E2F8, CSRP3-AS1 (H667D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2332875	NM_024680.4(E2F8):c.1193T>C (p.Ile398Thr)	CSRP3-AS1, E2F8 (I398T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2330137	NM_024680.4(E2F8):c.1115G>A (p.Arg372Gln)	CSRP3-AS1, E2F8 (R372Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2320745	NM_024680.4(E2F8):c.2147C>T (p.Pro716Leu)	CSRP3-AS1, E2F8 (P716L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2316698	NM_024680.4(E2F8):c.1178G>A (p.Arg393Gln)	CSRP3-AS1, E2F8 (R393Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2315257	NM_024680.4(E2F8):c.1988T>C (p.Leu663Pro)	E2F8, CSRP3-AS1 (L663P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2301280	NM_024680.4(E2F8):c.1769G>A (p.Gly590Glu)	CSRP3-AS1, E2F8 (G590E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2298113	NM_024680.4(E2F8):c.275A>C (p.Glu92Ala)	E2F8, CSRP3-AS1 (E92A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2291111	NM_024680.4(E2F8):c.146A>G (p.Lys49Arg)	E2F8, CSRP3-AS1 (K49R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2290545	NM_024680.4(E2F8):c.896A>C (p.His299Pro)	E2F8, CSRP3-AS1 (H299P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2280835	NM_024680.4(E2F8):c.2128G>A (p.Val710Ile)	CSRP3-AS1, E2F8 (V710I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2227241	NM_024680.4(E2F8):c.1843T>C (p.Ser615Pro)	CSRP3-AS1, E2F8 (S615P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2215681	NM_024680.4(E2F8):c.1108G>C (p.Val370Leu)	CSRP3-AS1, E2F8 (V370L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 790408	NM_024680.4(E2F8):c.2534A>G (p.Asn845Ser)	CSRP3-AS1, E2F8 (N845S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 789793	NM_024680.4(E2F8):c.1896C>T (p.Thr632=)	CSRP3-AS1, E2F8	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 789792	NM_024680.4(E2F8):c.2020A>G (p.Ile674Val)	CSRP3-AS1, E2F8 (I674V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 786190	NM_024680.4(E2F8):c.204T>C (p.Ser68=)	CSRP3-AS1, E2F8	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 781219	NM_024680.4(E2F8):c.78C>T (p.Thr26=)	CSRP3-AS1, E2F8	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 776601	NM_024680.4(E2F8):c.1073G>C (p.Ser358Thr)	CSRP3-AS1, E2F8 (S358T)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 747979	NM_024680.4(E2F8):c.2091G>A (p.Pro697=)	CSRP3-AS1, E2F8	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 742105	NM_024680.4(E2F8):c.1038C>T (p.Thr346=)	CSRP3-AS1, E2F8	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 709992	NM_024680.4(E2F8):c.2310C>T (p.Val770=)	CSRP3-AS1, E2F8	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 708138	NM_024680.4(E2F8):c.692T>C (p.Ile231Thr)	CSRP3-AS1, E2F8 (I231T)	Single nucleotide variant (missense variant)	not provided	GLikely benign

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Links from Gene

Items: 41