"Ambry Genetics"[submitter] AND "NME9"[gene] - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2346415	NM_001363941.2(ARMC8):c.1408G>A (p.Val470Ile)	ARMC8, NME9 (V397I +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129672	NM_001363941.2(ARMC8):c.1528A>G (p.Ser510Gly)	ARMC8, NME9 (S443G +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3129673	NM_001363941.2(ARMC8):c.1648A>G (p.Ser550Gly)	ARMC8, NME9 (S519G +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3315748	NM_001363941.2(ARMC8):c.1735A>C (p.Ile579Leu)	ARMC8, NME9 (I506L +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2277142	NM_001363941.2(ARMC8):c.1996A>G (p.Met666Val)	ARMC8, NME9 (M624V +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2459924	NM_001349018.2(NME9):c.919G>A (p.Ala307Thr)	NME9 (A268T +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472178	NM_001349018.2(NME9):c.845G>A (p.Arg282Gln)	NME9 (R192Q +4 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2404065	NM_001349018.2(NME9):c.832G>A (p.Val278Ile)	NME9 (V215I +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515563	NM_001349018.2(NME9):c.808G>T (p.Gly270Cys)	NME9 (G270C +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3200821	NM_001349018.2(NME9):c.782A>G (p.Gln261Arg)	NME9 (Q198R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384511	NM_001349018.2(NME9):c.764A>G (p.Asn255Ser)	NME9 (N255S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620374	NM_001349018.2(NME9):c.754C>T (p.Arg252Cys)	NME9 (R191C +4 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2281737	NM_001349018.2(NME9):c.742G>A (p.Val248Ile)	NME9 (V209I +4 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3300159	NM_001349018.2(NME9):c.640G>A (p.Ala214Thr)	NME9 (A153T +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3300158	NM_001349018.2(NME9):c.539T>C (p.Met180Thr)	NME9 (M117T +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542888	NM_001349018.2(NME9):c.430G>A (p.Gly144Arg)	NME9 (G144R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406497	NM_001349018.2(NME9):c.248C>A (p.Pro83Gln)	NME9 (P61Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2398024	NM_001349018.2(NME9):c.211C>T (p.Leu71Phe)	NME9 (L71F +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2380619	NM_001349018.2(NME9):c.200A>G (p.Glu67Gly)	NME9 (E16G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3200820	NM_001349018.2(NME9):c.184C>T (p.His62Tyr)	NME9 (H40Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2373069	NM_001349018.2(NME9):c.98A>C (p.Asp33Ala)	NME9 (D11A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 21