"Ambry Genetics"[submitter] AND "LIN9"[gene] - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2240885	NM_001366245.2(LIN9):c.1496A>G (p.Lys499Arg)	LIN9 (K406R +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2266054	NM_001366245.2(LIN9):c.1293G>A (p.Met431Ile)	LIN9 (M446I +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330093	NM_001366245.2(LIN9):c.1282C>G (p.Pro428Ala)	LIN9 (P410A +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118951	NM_001366245.2(LIN9):c.1237T>C (p.Cys413Arg)	LIN9 (C394R +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211006	NM_001366245.2(LIN9):c.1157G>A (p.Arg386Gln)	LIN9 (R334Q +7 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2515526	NM_001366245.2(LIN9):c.965C>T (p.Pro322Leu)	LIN9 (P322L +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3118956	NM_001366245.2(LIN9):c.914C>G (p.Pro305Arg)	LIN9 (P212R +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2496336	NM_001366245.2(LIN9):c.913C>A (p.Pro305Thr)	LIN9 (P212T +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603147	NM_001366245.2(LIN9):c.902T>C (p.Leu301Ser)	LIN9 (L301S +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388899	NM_001366245.2(LIN9):c.899G>A (p.Arg300Gln)	LIN9 (R281Q +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542613	NM_001366245.2(LIN9):c.890C>T (p.Thr297Ile)	LIN9 (T312I +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248646	NM_001366245.2(LIN9):c.868C>T (p.Arg290Trp)	LIN9 (R306W +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118955	NM_001366245.2(LIN9):c.796A>G (p.Ile266Val)	LIN9 (I173V +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2487162	NM_001366245.2(LIN9):c.671C>T (p.Thr224Met)	LIN9 (T239M +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303698	NM_001366245.2(LIN9):c.628A>G (p.Lys210Glu)	LIN9 (K225E +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118953	NM_001366245.2(LIN9):c.454A>G (p.Asn152Asp)	LIN9 (N133D +5 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460189	NM_001366245.2(LIN9):c.280A>G (p.Met94Val)	LIN9 (M94V +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2214738	NM_001366245.2(LIN9):c.253A>G (p.Met85Val)	LIN9 (M100V +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2604503	NM_001366245.2(LIN9):c.196G>C (p.Asp66His)	LIN9 (D14H +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2244595	NM_001366245.2(LIN9):c.130G>T (p.Gly44Cys)	LIN9 (G60C +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2533902	NM_001366245.2(LIN9):c.121G>A (p.Val41Ile)	LIN9 (V56I +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2333585	NM_001366245.2(LIN9):c.17A>G (p.Gln6Arg)	LIN9 (Q22R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3118954	NM_001366245.2(LIN9):c.10C>T (p.Leu4Phe)	LIN9 (L20F +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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Items: 23