"Ambry Genetics"[submitter] AND "MTMR9"[gene] - ClinVar

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Items: 73

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2542754	NM_015458.4(MTMR9):c.59C>A (p.Pro20His)	MTMR9 (P20H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216748	NM_015458.4(MTMR9):c.113T>C (p.Leu38Pro)	MTMR9 (L38P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2454449	NM_015458.4(MTMR9):c.169G>A (p.Ala57Thr)	MTMR9 (A57T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545047	NM_015458.4(MTMR9):c.235A>T (p.Ile79Phe)	MTMR9 (I79F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296734	NM_015458.4(MTMR9):c.240G>T (p.Gln80His)	MTMR9 (Q80H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610492	NM_015458.4(MTMR9):c.283T>A (p.Ser95Thr)	MTMR9 (S95T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471705	NM_015458.4(MTMR9):c.299C>T (p.Ser100Phe)	MTMR9 (S100F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533988	NM_015458.4(MTMR9):c.304C>G (p.Leu102Val)	MTMR9 (L102V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333115	NM_015458.4(MTMR9):c.307G>C (p.Asp103His)	MTMR9 (D103H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272594	NM_015458.4(MTMR9):c.328C>G (p.Pro110Ala)	MTMR9 (P110A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216819	NM_015458.4(MTMR9):c.341G>A (p.Arg114His)	MTMR9 (R114H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490393	NM_015458.4(MTMR9):c.356T>G (p.Val119Gly)	MTMR9 (V119G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305938	NM_015458.4(MTMR9):c.365A>G (p.Asp122Gly)	MTMR9 (D122G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216827	NM_015458.4(MTMR9):c.374A>G (p.His125Arg)	MTMR9 (H125R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2335865	NM_015458.4(MTMR9):c.407A>C (p.Tyr136Ser)	MTMR9 (Y136S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308868	NM_015458.4(MTMR9):c.425A>C (p.Glu142Ala)	MTMR9 (E142A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297996	NM_015458.4(MTMR9):c.440A>C (p.Tyr147Ser)	MTMR9 (Y147S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336723	NM_015458.4(MTMR9):c.460G>A (p.Val154Ile)	MTMR9 (V154I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216837	NM_015458.4(MTMR9):c.545G>A (p.Gly182Glu)	MTMR9 (G182E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216849	NM_015458.4(MTMR9):c.652G>C (p.Glu218Gln)	MTMR9 (E218Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619249	NM_015458.4(MTMR9):c.710G>A (p.Arg237Gln)	MTMR9 (R237Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495997	NM_015458.4(MTMR9):c.713C>G (p.Ser238Cys)	MTMR9 (S238C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216863	NM_015458.4(MTMR9):c.869A>G (p.His290Arg)	MTMR9 (H290R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547043	NM_015458.4(MTMR9):c.889A>G (p.Ser297Gly)	MTMR9 (S297G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216869	NM_015458.4(MTMR9):c.908A>G (p.Asn303Ser)	MTMR9 (N303S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216873	NM_015458.4(MTMR9):c.940A>G (p.Thr314Ala)	MTMR9 (T314A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3296735	NM_015458.4(MTMR9):c.949C>G (p.Leu317Val)	MTMR9 (L317V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513144	NM_015458.4(MTMR9):c.1027G>A (p.Val343Met)	MTMR9 (V343M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261048	NM_015458.4(MTMR9):c.1108C>A (p.Leu370Met)	MTMR9 (L370M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212860	NM_015458.4(MTMR9):c.1153T>A (p.Tyr385Asn)	LOC101929290, MTMR9 (Y385N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390466	NM_015458.4(MTMR9):c.1204G>T (p.Asp402Tyr)	LOC101929290, MTMR9 (D402Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463575	NM_015458.4(MTMR9):c.1239T>G (p.Cys413Trp)	LOC101929290, MTMR9 (C413W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249501	NM_015458.4(MTMR9):c.1258A>G (p.Asn420Asp)	LOC101929290, MTMR9 (N420D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274575	NM_015458.4(MTMR9):c.1294T>C (p.Ser432Pro)	LOC101929290, MTMR9 (S432P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216766	NM_015458.4(MTMR9):c.1299G>C (p.Gln433His)	LOC101929290, MTMR9 (Q433H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293799	NM_015458.4(MTMR9):c.1347G>C (p.Lys449Asn)	LOC101929290, MTMR9 (K449N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385504	NM_015458.4(MTMR9):c.1391C>G (p.Pro464Arg)	LOC101929290, MTMR9 (P464R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2560088	NM_015458.4(MTMR9):c.1395T>G (p.Ser465Arg)	LOC101929290, MTMR9 (S465R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216776	NM_015458.4(MTMR9):c.1436A>G (p.Asn479Ser)	LOC101929290, MTMR9 (N479S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296736	NM_015458.4(MTMR9):c.1438C>T (p.Leu480Phe)	LOC101929290, MTMR9 (L480F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216778	NM_015458.4(MTMR9):c.1462C>G (p.Pro488Ala)	LOC101929290, MTMR9 (P488A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387851	NM_015458.4(MTMR9):c.1555A>G (p.Ile519Val)	LOC101929290, MTMR9 (I519V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2261010	NM_015458.4(MTMR9):c.1592T>G (p.Ile531Ser)	LOC101929290, MTMR9 (I531S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3216786	NM_015458.4(MTMR9):c.1605G>T (p.Gln535His)	LOC101929290, MTMR9 (Q535H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2231029	NM_015458.4(MTMR9):c.1628A>T (p.Asp543Val)	LOC101929290, MTMR9 (D543V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272986	NM_015458.4(MTMR9):c.1645C>T (p.Pro549Ser)	LOC101929290, MTMR9 (P549S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3319658	NM_054028.2(SLC35G5):c.12T>A (p.Ser4Arg)	MTMR9, SLC35G5 (S4R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164464	NM_054028.2(SLC35G5):c.53C>T (p.Pro18Leu)	MTMR9, SLC35G5 (P18L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280887	NM_054028.2(SLC35G5):c.55C>A (p.Pro19Thr)	MTMR9, SLC35G5 (P19T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164466	NM_054028.2(SLC35G5):c.64C>G (p.Pro22Ala)	MTMR9, SLC35G5 (P22A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164469	NM_054028.2(SLC35G5):c.81G>C (p.Trp27Cys)	MTMR9, SLC35G5 (W27C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456963	NM_054028.2(SLC35G5):c.97C>G (p.Pro33Ala)	MTMR9, SLC35G5 (P33A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410102	NM_054028.2(SLC35G5):c.113A>G (p.Asn38Ser)	MTMR9, SLC35G5 (N38S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552017	NM_054028.2(SLC35G5):c.127G>T (p.Ala43Ser)	MTMR9, SLC35G5 (A43S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323112	NM_054028.2(SLC35G5):c.188A>G (p.Gln63Arg)	MTMR9, SLC35G5 (Q63R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2543238	NM_054028.2(SLC35G5):c.245C>G (p.Pro82Arg)	MTMR9, SLC35G5 (P82R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611245	NM_054028.2(SLC35G5):c.256C>G (p.Leu86Val)	MTMR9, SLC35G5 (L86V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465121	NM_054028.2(SLC35G5):c.280C>G (p.Leu94Val)	MTMR9, SLC35G5 (L94V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3319657	NM_054028.2(SLC35G5):c.292C>G (p.Pro98Ala)	MTMR9, SLC35G5 (P98A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346019	NM_054028.2(SLC35G5):c.337C>T (p.Leu113Phe)	MTMR9, SLC35G5 (L113F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164463	NM_054028.2(SLC35G5):c.388G>A (p.Ala130Thr)	MTMR9, SLC35G5 (A130T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509077	NM_054028.2(SLC35G5):c.389C>A (p.Ala130Asp)	MTMR9, SLC35G5 (A130D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2566757	NM_054028.2(SLC35G5):c.400C>T (p.Arg134Cys)	MTMR9, SLC35G5 (R134C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212595	NM_054028.2(SLC35G5):c.406G>T (p.Gly136Cys)	MTMR9, SLC35G5 (G136C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552541	NM_054028.2(SLC35G5):c.455A>G (p.Gln152Arg)	MTMR9, SLC35G5 (Q152R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255046	NM_054028.2(SLC35G5):c.529C>G (p.Leu177Val)	MTMR9, SLC35G5 (L177V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164465	NM_054028.2(SLC35G5):c.629A>T (p.Tyr210Phe)	MTMR9, SLC35G5 (Y210F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164467	NM_054028.2(SLC35G5):c.673C>G (p.Leu225Val)	MTMR9, SLC35G5 (L225V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164468	NM_054028.2(SLC35G5):c.745G>A (p.Asp249Asn)	MTMR9, SLC35G5 (D249N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3319656	NM_054028.2(SLC35G5):c.773C>T (p.Ala258Val)	MTMR9, SLC35G5 (A258V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349543	NM_054028.2(SLC35G5):c.787G>A (p.Ala263Thr)	MTMR9, SLC35G5 (A263T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516273	NM_054028.2(SLC35G5):c.884T>C (p.Ile295Thr)	MTMR9, SLC35G5 (I295T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300675	NM_054028.2(SLC35G5):c.900G>C (p.Met300Ile)	MTMR9, SLC35G5 (M300I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 73