"Ambry Genetics"[submitter] AND "LINC02908"[gene] - ClinVar

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Search results

Items: 47

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2411948	NM_212533.3(ABCA2):c.125G>A (p.Arg42Gln)	ABCA2, LINC02908 (R42Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242031	NM_212533.3(ABCA2):c.79G>C (p.Gly27Arg)	ABCA2, LINC02908 (G27R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280214	NM_004479.4(FUT7):c.1012G>A (p.Gly338Ser)	FUT7, LINC02908 (G338S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553590	NM_004479.4(FUT7):c.971A>T (p.Tyr324Phe)	FUT7, LINC02908 (Y324F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280803	NM_004479.4(FUT7):c.958A>C (p.Ile320Leu)	FUT7, LINC02908 (I320L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324647	NM_004479.4(FUT7):c.940C>T (p.Arg314Trp)	FUT7, LINC02908 (R314W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280219	NM_004479.4(FUT7):c.934G>A (p.Asp312Asn)	FUT7, LINC02908 (D312N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280218	NM_004479.4(FUT7):c.919G>A (p.Val307Met)	FUT7, LINC02908 (V307M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280217	NM_004479.4(FUT7):c.905G>A (p.Arg302His)	FUT7, LINC02908 (R302H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542863	NM_004479.4(FUT7):c.893T>G (p.Phe298Cys)	FUT7, LINC02908 (F298C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390405	NM_004479.4(FUT7):c.881G>A (p.Arg294Gln)	FUT7, LINC02908 (R294Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590581	NM_004479.4(FUT7):c.847C>G (p.Leu283Val)	FUT7, LINC02908 (L283V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295731	NM_004479.4(FUT7):c.827A>G (p.Asp276Gly)	FUT7, LINC02908 (D276G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549981	NM_004479.4(FUT7):c.749C>T (p.Thr250Ile)	FUT7, LINC02908 (T250I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337605	NM_004479.4(FUT7):c.728G>C (p.Arg243Pro)	FUT7, LINC02908 (R243P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508502	NM_004479.4(FUT7):c.713C>T (p.Thr238Met)	FUT7, LINC02908 (T238M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2400814	NM_004479.4(FUT7):c.668G>A (p.Arg223His)	FUT7, LINC02908 (R223H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097533	NM_004479.4(FUT7):c.634G>A (p.Ala212Thr)	FUT7, LINC02908 (A212T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2549386	NM_004479.4(FUT7):c.610C>T (p.Arg204Cys)	FUT7, LINC02908 (R204C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097530	NM_004479.4(FUT7):c.601G>A (p.Val201Ile)	FUT7, LINC02908 (V201I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457239	NM_004479.4(FUT7):c.595G>A (p.Val199Met)	FUT7, LINC02908 (V199M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460188	NM_004479.4(FUT7):c.592C>T (p.Arg198Trp)	FUT7, LINC02908 (R198W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324526	NM_004479.4(FUT7):c.581C>T (p.Ala194Val)	FUT7, LINC02908 (A194V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3097529	NM_004479.4(FUT7):c.580G>A (p.Ala194Thr)	FUT7, LINC02908 (A194T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271352	NM_004479.4(FUT7):c.494C>T (p.Pro165Leu)	FUT7, LINC02908 (P165L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280213	NM_004479.4(FUT7):c.488C>T (p.Ser163Leu)	FUT7, LINC02908 (S163L)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2596558	NM_004479.4(FUT7):c.463C>T (p.Arg155Cys)	FUT7, LINC02908 (R155C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213249	NM_004479.4(FUT7):c.436G>A (p.Asp146Asn)	FUT7, LINC02908 (D146N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097528	NM_004479.4(FUT7):c.434G>A (p.Arg145His)	FUT7, LINC02908 (R145H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2391124	NM_004479.4(FUT7):c.302G>A (p.Arg101Gln)	FUT7, LINC02908 (R101Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341359	NM_004479.4(FUT7):c.271G>A (p.Val91Met)	FUT7, LINC02908 (V91M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280215	NM_004479.4(FUT7):c.245G>A (p.Arg82Gln)	FUT7, LINC02908 (R82Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316433	NM_004479.4(FUT7):c.242A>G (p.Asn81Ser)	FUT7, LINC02908 (N81S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272304	NM_004479.4(FUT7):c.233T>G (p.Leu78Arg)	FUT7, LINC02908 (L78R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097527	NM_004479.4(FUT7):c.224G>A (p.Arg75His)	FUT7, LINC02908 (R75H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3280222	NM_004479.4(FUT7):c.197A>T (p.Asp66Val)	FUT7, LINC02908 (D66V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280212	NM_004479.4(FUT7):c.122C>T (p.Pro41Leu)	FUT7, LINC02908 (P41L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280216	NM_004479.4(FUT7):c.112C>T (p.Arg38Trp)	FUT7, LINC02908 (R38W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245270	NM_004479.4(FUT7):c.91T>C (p.Trp31Arg)	FUT7, LINC02908 (W31R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2331288	NM_004479.4(FUT7):c.77C>T (p.Ala26Val)	FUT7, LINC02908 (A26V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3097532	NM_004479.4(FUT7):c.62T>C (p.Val21Ala)	FUT7, LINC02908 (V21A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2408579	NM_004479.4(FUT7):c.28C>T (p.Arg10Trp)	FUT7, LINC02908 (R10W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3280220	NM_004479.4(FUT7):c.5A>G (p.Asn2Ser)	FUT7, LINC02908 (N2S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118979	NR_171031.1(LINC02908):n.1528G>T	LINC02908	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3118980	NR_171031.1(LINC02908):n.1533C>T	LINC02908	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3118982	NR_171031.1(LINC02908):n.1588G>T	LINC02908	Single nucleotide variant (non-coding transcript variant)	not specified	GUncertain significance
Select item 3118981	NR_171031.1(LINC02908):n.1819G>A	LINC02908	Single nucleotide variant (non-coding transcript variant)	not specified	GLikely benign

ClinVar

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Items: 47