"Ambry Genetics"[submitter] AND "LY6K"[gene] - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2374580	NM_017527.4(LY6K):c.5C>T (p.Ala2Val)	LY6K (A2V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533378	NM_017527.4(LY6K):c.13G>C (p.Ala5Pro)	LY6K (A5P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3292354	NM_017527.4(LY6K):c.46T>A (p.Trp16Arg)	LY6K (W16R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544794	NM_017527.4(LY6K):c.50C>A (p.Thr17Lys)	LY6K (T17K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330008	NM_017527.4(LY6K):c.61C>G (p.Leu21Val)	LY6K (L21V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232238	NM_017527.4(LY6K):c.110G>C (p.Gly37Ala)	LY6K (G37A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2588934	NM_017527.4(LY6K):c.114C>A (p.Asp38Glu)	LY6K (D38E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3121628	NM_017527.4(LY6K):c.152C>T (p.Thr51Ile)	LY6K (T51I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2221202	NM_017527.4(LY6K):c.215T>A (p.Val72Glu)	LY6K (V72E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374312	NM_017527.4(LY6K):c.229C>T (p.Arg77Cys)	LNCOC1, LY6K (R77C)	Single nucleotide variant (non-coding transcript variant +3 more)	not specified	GUncertain significance
Select item 2491131	NM_017527.4(LY6K):c.257C>G (p.Ser86Cys)	LNCOC1, LY6K (S86C)	Single nucleotide variant (non-coding transcript variant +3 more)	not specified	GUncertain significance
Select item 2350242	NM_017527.4(LY6K):c.259G>A (p.Ala87Thr)	LNCOC1, LY6K (R76H +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2330588	NM_017527.4(LY6K):c.295G>A (p.Glu99Lys)	LNCOC1, LY6K (E99K +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2323832	NM_017527.4(LY6K):c.301C>T (p.Arg101Trp)	LNCOC1, LY6K (R101W +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2348041	NM_017527.4(LY6K):c.308T>C (p.Leu103Pro)	LNCOC1, LY6K (L103P)	Single nucleotide variant (non-coding transcript variant +3 more)	not specified	GUncertain significance
Select item 2348042	NM_017527.4(LY6K):c.328T>C (p.Phe110Leu)	LNCOC1, LY6K (F110L +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3292352	NM_017527.4(LY6K):c.346T>C (p.Cys116Arg)	LNCOC1, LY6K (C116R +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3121629	NM_017527.4(LY6K):c.356G>A (p.Arg119His)	LNCOC1, LY6K (R119H)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2523162	NM_017527.4(LY6K):c.380C>G (p.Pro127Arg)	LNCOC1, LY6K (P127R)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2358595	NM_017527.4(LY6K):c.481G>A (p.Gly161Ser)	LNCOC1, LY6K (G161S)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance

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Items: 20