"Ambry Genetics"[submitter] AND "XKR9"[gene] - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2359905	NM_001011720.2(XKR9):c.204G>C (p.Lys68Asn)	XKR9 (K68N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2239047	NM_001011720.2(XKR9):c.260G>A (p.Gly87Glu)	XKR9 (G87E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3191175	NM_001011720.2(XKR9):c.273G>T (p.Arg91Ser)	XKR9 (R91S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2307831	NM_001011720.2(XKR9):c.290A>G (p.Lys97Arg)	XKR9 (K97R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2478945	NM_001011720.2(XKR9):c.305C>A (p.Ala102Glu)	XKR9 (A102E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2243438	NM_001011720.2(XKR9):c.314A>C (p.Lys105Thr)	XKR9 (K105T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3191176	NM_001011720.2(XKR9):c.339C>A (p.Phe113Leu)	XKR9 (F113L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2528800	NM_001011720.2(XKR9):c.351A>C (p.Gln117His)	XKR9 (Q117H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2372297	NM_001011720.2(XKR9):c.358C>A (p.Leu120Ile)	XKR9 (L120I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3191178	NM_001011720.2(XKR9):c.431G>A (p.Cys144Tyr)	XKR9 (C12Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191179	NM_001011720.2(XKR9):c.458T>C (p.Ile153Thr)	XKR9 (I153T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224883	NM_001011720.2(XKR9):c.479C>T (p.Ala160Val)	XKR9 (A160V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333458	NM_001011720.2(XKR9):c.488G>T (p.Ser163Ile)	XKR9 (S31I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347626	NM_001011720.2(XKR9):c.499G>A (p.Ala167Thr)	XKR9 (A35T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553739	NM_001011720.2(XKR9):c.535A>G (p.Thr179Ala)	XKR9 (T179A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333457	NM_001011720.2(XKR9):c.536C>G (p.Thr179Ser)	XKR9 (T179S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191180	NM_001011720.2(XKR9):c.549A>C (p.Gln183His)	XKR9 (Q183H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191181	NM_001011720.2(XKR9):c.604A>C (p.Lys202Gln)	XKR9 (K70Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191182	NM_001011720.2(XKR9):c.651G>A (p.Met217Ile)	XKR9 (M217I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2527861	NM_001011720.2(XKR9):c.674T>A (p.Phe225Tyr)	XKR9 (F93Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270542	NM_001011720.2(XKR9):c.737C>T (p.Ala246Val)	XKR9 (A246V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397315	NM_001011720.2(XKR9):c.787T>C (p.Tyr263His)	XKR9 (Y131H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191183	NM_001011720.2(XKR9):c.823T>G (p.Phe275Val)	XKR9 (F275V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2512579	NM_001011720.2(XKR9):c.908C>G (p.Thr303Ser)	XKR9 (T303S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3191184	NM_001011720.2(XKR9):c.919G>A (p.Val307Ile)	XKR9 (V307I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333455	NM_001011720.2(XKR9):c.934A>G (p.Ile312Val)	XKR9 (I180V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305836	NM_001011720.2(XKR9):c.1000C>T (p.Leu334Phe)	XKR9 (L202F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 27