"Ambry Genetics"[submitter] AND "XPO6"[gene] - ClinVar

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Items: 34

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3333495	NM_015171.4(XPO6):c.3257G>A (p.Arg1086Gln)	XPO6 (R1086Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333494	NM_015171.4(XPO6):c.2977A>G (p.Ile993Val)	XPO6 (I993V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191255	NM_015171.4(XPO6):c.2974G>A (p.Asp992Asn)	XPO6 (D978N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2234877	NM_015171.4(XPO6):c.2940C>G (p.Ile980Met)	XPO6 (I980M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191254	NM_015171.4(XPO6):c.2746G>A (p.Ala916Thr)	XPO6 (A916T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397309	NM_015171.4(XPO6):c.2702A>G (p.Gln901Arg)	XPO6 (Q901R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2569650	NM_015171.4(XPO6):c.2540G>A (p.Arg847Gln)	XPO6 (R833Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333498	NM_015171.4(XPO6):c.2521T>G (p.Phe841Val)	XPO6 (F827V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322691	NM_015171.4(XPO6):c.2459T>G (p.Val820Gly)	XPO6 (V806G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204546	NM_015171.4(XPO6):c.2371G>A (p.Val791Ile)	XPO6 (V791I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516070	NM_015171.4(XPO6):c.2281G>T (p.Asp761Tyr)	XPO6 (D747Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235217	NM_015171.4(XPO6):c.2171G>A (p.Arg724Gln)	XPO6 (R710Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333499	NM_015171.4(XPO6):c.2089C>T (p.Pro697Ser)	XPO6 (P683S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457571	NM_015171.4(XPO6):c.1940C>T (p.Thr647Met)	XPO6 (T633M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191253	NM_015171.4(XPO6):c.1931G>A (p.Arg644Gln)	XPO6 (R630Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353357	NM_015171.4(XPO6):c.1625C>T (p.Thr542Met)	XPO6 (T528M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191252	NM_015171.4(XPO6):c.1591G>C (p.Val531Leu)	XPO6 (V531L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191251	NM_015171.4(XPO6):c.1463G>A (p.Arg488Gln)	XPO6 (R488Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2557839	NM_015171.4(XPO6):c.1409T>G (p.Leu470Arg)	XPO6 (L470R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191250	NM_015171.4(XPO6):c.1339G>A (p.Glu447Lys)	XPO6 (E433K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2624150	NM_015171.4(XPO6):c.1316A>T (p.Lys439Met)	XPO6 (K425M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333493	NM_015171.4(XPO6):c.1229C>T (p.Thr410Ile)	XPO6 (T410I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191249	NM_015171.4(XPO6):c.1189T>C (p.Phe397Leu)	XPO6 (F397L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310365	NM_015171.4(XPO6):c.1102A>G (p.Ile368Val)	XPO6 (I354V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244503	NM_015171.4(XPO6):c.928G>C (p.Val310Leu)	XPO6 (V310L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213144	NM_015171.4(XPO6):c.703A>T (p.Ile235Phe)	XPO6 (I221F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210972	NM_015171.4(XPO6):c.640A>T (p.Ser214Cys)	XPO6 (S214C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217185	NM_015171.4(XPO6):c.626C>T (p.Pro209Leu)	XPO6 (P209L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333492	NM_015171.4(XPO6):c.623C>A (p.Ser208Tyr)	XPO6 (S194Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191258	NM_015171.4(XPO6):c.586G>A (p.Asp196Asn)	XPO6 (D182N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2514282	NM_015171.4(XPO6):c.566G>A (p.Gly189Asp)	XPO6 (G175D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191256	NM_015171.4(XPO6):c.482G>A (p.Arg161His)	XPO6 (R161H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191259	NM_015171.4(XPO6):c.98A>G (p.Glu33Gly)	XPO6 (E33G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333497	NM_015171.4(XPO6):c.85C>T (p.Arg29Cys)	XPO6 (R29C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 34