AIFM3[gene] and "single gene"[properties] - ClinVar

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Items: 42

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3102734	NM_001386814.1(AIFM3):c.71G>A (p.Arg24Gln)	AIFM3 (R24Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2276228	NM_001386814.1(AIFM3):c.83A>C (p.Glu28Ala)	AIFM3 (E28A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2204254	NM_001386814.1(AIFM3):c.89C>T (p.Ser30Leu)	AIFM3 (S30L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102747	NM_001386814.1(AIFM3):c.94A>T (p.Ser32Cys)	AIFM3 (S32C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3278987	NM_001386814.1(AIFM3):c.122A>G (p.Gln41Arg)	AIFM3 (Q47R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102690	NM_001386814.1(AIFM3):c.139C>T (p.Arg47Cys)	AIFM3 (R47C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2621207	NM_001386814.1(AIFM3):c.161G>T (p.Arg54Leu)	AIFM3 (R54L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2274591	NM_001386814.1(AIFM3):c.310G>T (p.Ala104Ser)	AIFM3 (A110S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364100	NM_001386814.1(AIFM3):c.313C>G (p.Leu105Val)	AIFM3 (L105V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553751	NM_001386814.1(AIFM3):c.322A>G (p.Lys108Glu)	AIFM3 (K108E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278983	NM_001386814.1(AIFM3):c.329C>T (p.Pro110Leu)	AIFM3 (P116L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529294	NM_001386814.1(AIFM3):c.343C>T (p.Pro115Ser)	AIFM3 (P121S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522726	NM_001386814.1(AIFM3):c.367C>T (p.Arg123Cys)	AIFM3 (R123C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102717	NM_001386814.1(AIFM3):c.373C>T (p.Arg125Trp)	AIFM3 (R131W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2611713	NM_001386814.1(AIFM3):c.584C>T (p.Thr195Ile)	AIFM3 (T195I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2530925	NM_001386814.1(AIFM3):c.593T>A (p.Leu198His)	AIFM3 (L204H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2476968	NM_001386814.1(AIFM3):c.628G>A (p.Ala210Thr)	AIFM3 (A210T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102725	NM_001386814.1(AIFM3):c.641G>A (p.Arg214Gln)	AIFM3 (R214Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2410462	NM_001386814.1(AIFM3):c.686G>A (p.Arg229Gln)	AIFM3 (R229Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2293760	NM_001386814.1(AIFM3):c.715A>T (p.Ser239Cys)	AIFM3 (S239C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2373121	NM_001386814.1(AIFM3):c.911T>A (p.Leu304Gln)	AIFM3 (L304Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102744	NM_001386814.1(AIFM3):c.940G>A (p.Val314Met)	AIFM3 (V314M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2652925	NM_001386814.1(AIFM3):c.951C>T (p.Ile317=)	AIFM3	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3102750	NM_001386814.1(AIFM3):c.952C>T (p.Arg318Trp)	AIFM3 (R318W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102757	NM_001386814.1(AIFM3):c.953G>A (p.Arg318Gln)	AIFM3 (R324Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102764	NM_001386814.1(AIFM3):c.976G>A (p.Val326Met)	AIFM3 (V332M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2520057	NM_001386814.1(AIFM3):c.1003G>A (p.Val335Met)	AIFM3 (V341M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2511745	NM_001386814.1(AIFM3):c.1012G>A (p.Val338Met)	AIFM3 (V344M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3278981	NM_001386814.1(AIFM3):c.1028T>C (p.Leu343Pro)	AIFM3 (L349P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102662	NM_001386814.1(AIFM3):c.1064C>T (p.Ala355Val)	AIFM3 (A355V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2598059	NM_001386814.1(AIFM3):c.1094A>T (p.Glu365Val)	AIFM3 (E365V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2454278	NM_001386814.1(AIFM3):c.1097C>T (p.Thr366Met)	AIFM3 (T366M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102676	NM_001386814.1(AIFM3):c.1103T>G (p.Phe368Cys)	AIFM3 (F368C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102680	NM_001386814.1(AIFM3):c.1124G>A (p.Arg375His)	AIFM3 (R381H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102681	NM_001386814.1(AIFM3):c.1133G>A (p.Arg378His)	AIFM3 (R378H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2606695	NM_001386814.1(AIFM3):c.1177A>G (p.Met393Val)	AIFM3 (M399V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2323364	NM_001386814.1(AIFM3):c.1178T>G (p.Met393Arg)	AIFM3 (M399R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2399645	NM_001386814.1(AIFM3):c.1222A>G (p.Lys408Glu)	AIFM3 (K414E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3102689	NM_001386814.1(AIFM3):c.1252G>A (p.Val418Met)	AIFM3 (V424M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2538225	NM_001386814.1(AIFM3):c.1546G>A (p.Ala516Thr)	AIFM3 (A516T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2407834	NM_001386814.1(AIFM3):c.1558A>G (p.Lys520Glu)	AIFM3 (K520E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2217845	NM_001386814.1(AIFM3):c.1693C>A (p.Pro565Thr)	AIFM3 (P565T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 42