"Ambry Genetics"[submitter] AND "RUNDC3B"[gene] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2325116	NM_001134405.2(RUNDC3B):c.38G>C (p.Arg13Pro)	ABCB1, RUNDC3B (R13P)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2245358	NM_001134405.2(RUNDC3B):c.40G>A (p.Gly14Ser)	ABCB1, RUNDC3B (G14S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2399124	NM_001134405.2(RUNDC3B):c.43G>A (p.Gly15Ser)	ABCB1, RUNDC3B (G15S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2487482	NM_001134405.2(RUNDC3B):c.218T>G (p.Ile73Ser)	ABCB1, RUNDC3B (I73S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3157194	NM_001134405.2(RUNDC3B):c.239-6464A>T	ABCB1, RUNDC3B (Q96H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3315802	NM_001134405.2(RUNDC3B):c.265A>T (p.Ser89Cys)	ABCB1, RUNDC3B (S89C +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2480928	NM_001134405.2(RUNDC3B):c.271C>T (p.Arg91Cys)	ABCB1, RUNDC3B (R108C +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2308222	NM_001134405.2(RUNDC3B):c.305G>A (p.Arg102Gln)	ABCB1, RUNDC3B (R102Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2336322	NM_001134405.2(RUNDC3B):c.329G>A (p.Cys110Tyr)	ABCB1, RUNDC3B (C127Y +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2557052	NM_001134405.2(RUNDC3B):c.378A>T (p.Arg126Ser)	ABCB1, RUNDC3B (R126S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2235411	NM_001134405.2(RUNDC3B):c.455C>A (p.Thr152Asn)	ABCB1, RUNDC3B (T38N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2624229	NM_001134405.2(RUNDC3B):c.713G>T (p.Gly238Val)	RUNDC3B (G237V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3157195	NM_001134405.2(RUNDC3B):c.770A>T (p.Gln257Leu)	RUNDC3B (Q143L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547326	NM_001134405.2(RUNDC3B):c.774G>C (p.Lys258Asn)	RUNDC3B (K275N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519613	NM_001134405.2(RUNDC3B):c.892G>A (p.Asp298Asn)	RUNDC3B (D184N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3315801	NM_001134405.2(RUNDC3B):c.901C>A (p.His301Asn)	RUNDC3B (H300N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3315800	NM_001134405.2(RUNDC3B):c.931A>G (p.Ile311Val)	RUNDC3B (I328V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611966	NM_001134405.2(RUNDC3B):c.989G>A (p.Arg330Lys)	RUNDC3B (R329K +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2329922	NM_001134405.2(RUNDC3B):c.1010T>C (p.Leu337Pro)	RUNDC3B (L223P +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2212949	NM_001134405.2(RUNDC3B):c.1084C>G (p.His362Asp)	RUNDC3B (H361D +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2606187	NM_001134405.2(RUNDC3B):c.1120C>T (p.Leu374Phe)	RUNDC3B (L260F +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376686	NM_001134405.2(RUNDC3B):c.1144A>G (p.Ser382Gly)	RUNDC3B (S333G +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598902	NM_001134405.2(RUNDC3B):c.1156A>G (p.Thr386Ala)	RUNDC3B (T272A +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480460	NM_001134405.2(RUNDC3B):c.1190A>T (p.Asp397Val)	RUNDC3B (D348V +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595766	NM_001134405.2(RUNDC3B):c.1298C>G (p.Thr433Arg)	RUNDC3B (T319R +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 25