"Ambry Genetics"[submitter] AND "FNDC3A"[gene] - ClinVar

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Items: 48

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2377041	NM_001079673.2(FNDC3A):c.46A>G (p.Ser16Gly)	FNDC3A (S16G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2544544	NM_001079673.2(FNDC3A):c.59T>G (p.Leu20Arg)	FNDC3A (L20R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2617365	NM_001079673.2(FNDC3A):c.115G>A (p.Val39Ile)	FNDC3A (V39I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2407894	NM_001079673.2(FNDC3A):c.165G>C (p.Gln55His)	FNDC3A (Q55H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096062	NM_001079673.2(FNDC3A):c.244G>A (p.Ala82Thr)	FNDC3A (A26T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2345253	NM_001079673.2(FNDC3A):c.355C>G (p.Leu119Val)	FNDC3A (L63V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2482087	NM_001079673.2(FNDC3A):c.404A>C (p.His135Pro)	FNDC3A (H135P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2609859	NM_001079673.2(FNDC3A):c.481G>A (p.Gly161Arg)	FNDC3A (G161R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096069	NM_001079673.2(FNDC3A):c.496C>T (p.His166Tyr)	FNDC3A (H166Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096070	NM_001079673.2(FNDC3A):c.499T>G (p.Ser167Ala)	FNDC3A (S111A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2610561	NM_001079673.2(FNDC3A):c.536C>G (p.Ser179Cys)	FNDC3A (S123C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2231131	NM_001079673.2(FNDC3A):c.538A>T (p.Ser180Cys)	FNDC3A (S180C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2293230	NM_001079673.2(FNDC3A):c.584G>A (p.Gly195Glu)	FNDC3A (G195E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2529999	NM_001079673.2(FNDC3A):c.679G>C (p.Ala227Pro)	FNDC3A (A171P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2208752	NM_001079673.2(FNDC3A):c.742G>A (p.Val248Ile)	FNDC3A (V248I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2398471	NM_001079673.2(FNDC3A):c.766G>C (p.Asp256His)	FNDC3A (D200H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096071	NM_001079673.2(FNDC3A):c.769G>A (p.Glu257Lys)	FNDC3A (E201K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2291384	NM_001079673.2(FNDC3A):c.881A>G (p.Asn294Ser)	FNDC3A (N238S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2493924	NM_001079673.2(FNDC3A):c.1006G>A (p.Asp336Asn)	FNDC3A (D280N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2246483	NM_001079673.2(FNDC3A):c.1136T>C (p.Ile379Thr)	FNDC3A (I323T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2210694	NM_001079673.2(FNDC3A):c.1142A>G (p.Asn381Ser)	FNDC3A (N325S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096055	NM_001079673.2(FNDC3A):c.1144C>T (p.Arg382Trp)	FNDC3A (R326W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2317737	NM_001079673.2(FNDC3A):c.1178C>T (p.Ala393Val)	FNDC3A (A337V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096057	NM_001079673.2(FNDC3A):c.1366G>C (p.Glu456Gln)	FNDC3A (E400Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096058	NM_001079673.2(FNDC3A):c.1378T>C (p.Tyr460His)	FNDC3A (Y460H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2491872	NM_001079673.2(FNDC3A):c.1507T>G (p.Leu503Val)	FNDC3A (L447V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2558601	NM_001079673.2(FNDC3A):c.1579G>T (p.Val527Leu)	FNDC3A (V527L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2231171	NM_001079673.2(FNDC3A):c.1712C>T (p.Ser571Leu)	FNDC3A (S571L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2483563	NM_001079673.2(FNDC3A):c.1879C>G (p.Arg627Gly)	FNDC3A (R571G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096059	NM_001079673.2(FNDC3A):c.2053C>T (p.Pro685Ser)	FNDC3A (P629S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2605958	NM_001079673.2(FNDC3A):c.2100A>C (p.Glu700Asp)	FNDC3A (E644D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2617366	NM_001079673.2(FNDC3A):c.2206C>T (p.Arg736Cys)	FNDC3A (R680C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2385493	NM_001079673.2(FNDC3A):c.2210C>T (p.Ala737Val)	FNDC3A (A681V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2296639	NM_001079673.2(FNDC3A):c.2289G>C (p.Lys763Asn)	FNDC3A (K707N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096061	NM_001079673.2(FNDC3A):c.2366T>C (p.Val789Ala)	FNDC3A (V789A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2599960	NM_001079673.2(FNDC3A):c.2590G>A (p.Asp864Asn)	FNDC3A (D864N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096063	NM_001079673.2(FNDC3A):c.2751T>G (p.Asn917Lys)	FNDC3A (N917K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2306324	NM_001079673.2(FNDC3A):c.2816T>C (p.Phe939Ser)	FNDC3A (F883S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096064	NM_001079673.2(FNDC3A):c.2941A>G (p.Thr981Ala)	FNDC3A (T981A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2556937	NM_001079673.2(FNDC3A):c.3113A>G (p.Tyr1038Cys)	FNDC3A (Y1038C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096065	NM_001079673.2(FNDC3A):c.3122C>G (p.Thr1041Ser)	FNDC3A (T1041S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3096068	NM_001079673.2(FNDC3A):c.3206G>C (p.Cys1069Ser)	FNDC3A (C1013S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2399510	NM_001079673.2(FNDC3A):c.3310C>T (p.Arg1104Trp)	FNDC3A (R1048W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2454622	NM_001079673.2(FNDC3A):c.3320G>A (p.Ser1107Asn)	FNDC3A (S1051N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2237869	NM_001079673.2(FNDC3A):c.3425T>C (p.Leu1142Pro)	FNDC3A (L1142P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2367412	NM_001079673.2(FNDC3A):c.3494G>A (p.Arg1165Gln)	FNDC3A (R1109Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2333568	NM_001079673.2(FNDC3A):c.3506G>A (p.Ser1169Asn)	FNDC3A (S1169N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2606933	NM_001079673.2(FNDC3A):c.3548T>G (p.Phe1183Cys)	FNDC3A (F1183C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 48