"Ambry Genetics"[submitter] AND "SLC9A9"[gene] - ClinVar

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Items: 42

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3320299	NM_173653.4(SLC9A9):c.1892A>G (p.Tyr631Cys)	SLC9A9 (Y631C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351859	NM_173653.4(SLC9A9):c.1879G>A (p.Gly627Ser)	SLC9A9 (G627S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457802	NM_173653.4(SLC9A9):c.1865A>G (p.Tyr622Cys)	SLC9A9 (Y622C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358201	NM_173653.4(SLC9A9):c.1852A>G (p.Lys618Glu)	SLC9A9 (K618E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320303	NM_173653.4(SLC9A9):c.1837C>T (p.Pro613Ser)	SLC9A9 (P613S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1013232	NM_173653.4(SLC9A9):c.1808C>A (p.Ala603Glu)	SLC9A9 (A603E)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3165736	NM_173653.4(SLC9A9):c.1801C>T (p.Pro601Ser)	SLC9A9 (P601S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405963	NM_173653.4(SLC9A9):c.1766T>C (p.Ile589Thr)	SLC9A9 (I589T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295832	NM_173653.4(SLC9A9):c.1730A>G (p.Asp577Gly)	SLC9A9 (D577G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341596	NM_173653.4(SLC9A9):c.1706A>T (p.Tyr569Phe)	SLC9A9 (Y569F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320296	NM_173653.4(SLC9A9):c.1667G>A (p.Cys556Tyr)	SLC9A9 (C556Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165735	NM_173653.4(SLC9A9):c.1666T>C (p.Cys556Arg)	SLC9A9 (C556R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2541334	NM_173653.4(SLC9A9):c.1657C>T (p.Pro553Ser)	SLC9A9 (P553S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165734	NM_173653.4(SLC9A9):c.1634G>A (p.Gly545Asp)	SLC9A9 (G545D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320298	NM_173653.4(SLC9A9):c.1601A>C (p.His534Pro)	SLC9A9 (H534P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2313710	NM_173653.4(SLC9A9):c.1593C>G (p.Ser531Arg)	SLC9A9 (S531R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320300	NM_173653.4(SLC9A9):c.1574T>C (p.Leu525Pro)	SLC9A9 (L525P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320301	NM_173653.4(SLC9A9):c.1556A>G (p.Lys519Arg)	SLC9A9 (K519R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481816	NM_173653.4(SLC9A9):c.1528G>A (p.Ala510Thr)	SLC9A9 (A510T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320302	NM_173653.4(SLC9A9):c.1518A>C (p.Gln506His)	SLC9A9 (Q506H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165733	NM_173653.4(SLC9A9):c.1482C>A (p.Asp494Glu)	SLC9A9 (D494E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165732	NM_173653.4(SLC9A9):c.1478T>C (p.Val493Ala)	SLC9A9 (V493A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207265	NM_173653.4(SLC9A9):c.1397T>C (p.Leu466Pro)	SLC9A9 (L466P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165731	NM_173653.4(SLC9A9):c.1378A>G (p.Met460Val)	SLC9A9 (M460V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458759	NM_173653.4(SLC9A9):c.1351C>T (p.Arg451Trp)	SLC9A9 (R451W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220110	NM_173653.4(SLC9A9):c.1345G>A (p.Ala449Thr)	SLC9A9 (A449T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2273016	NM_173653.4(SLC9A9):c.1328C>T (p.Ala443Val)	SLC9A9 (A443V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2281804	NM_173653.4(SLC9A9):c.1214T>G (p.Phe405Cys)	SLC9A9 (F405C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456946	NM_173653.4(SLC9A9):c.1003A>T (p.Ile335Leu)	SLC9A9 (I335L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165738	NM_173653.4(SLC9A9):c.926C>T (p.Pro309Leu)	SLC9A9 (P309L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270906	NM_173653.4(SLC9A9):c.886A>G (p.Thr296Ala)	SLC9A9 (T296A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3165737	NM_173653.4(SLC9A9):c.850G>A (p.Gly284Ser)	SLC9A9 (G284S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349585	NM_173653.4(SLC9A9):c.847G>A (p.Ala283Thr)	SLC9A9 (A283T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2613564	NM_173653.4(SLC9A9):c.838G>A (p.Gly280Arg)	SLC9A9 (G280R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216211	NM_173653.4(SLC9A9):c.805G>A (p.Ala269Thr)	SLC9A9 (A269T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3320297	NM_173653.4(SLC9A9):c.793G>A (p.Ala265Thr)	SLC9A9 (A265T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2292289	NM_173653.4(SLC9A9):c.751A>C (p.Thr251Pro)	SLC9A9 (T251P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475911	NM_173653.4(SLC9A9):c.529A>G (p.Ile177Val)	SLC9A9 (I177V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395154	NM_173653.4(SLC9A9):c.491C>T (p.Thr164Met)	SLC9A9 (T164M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2623168	NM_173653.4(SLC9A9):c.436G>A (p.Ala146Thr)	SLC9A9 (A146T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231481	NM_173653.4(SLC9A9):c.129T>A (p.Asn43Lys)	SLC9A9 (N43K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2263850	NM_173653.4(SLC9A9):c.55C>G (p.Gln19Glu)	SLC9A9 (Q19E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 42