MTG1[gene] and "single gene"[properties] - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2540919	NM_138384.4(MTG1):c.125T>C (p.Met42Thr)	MTG1 (M42T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374355	NM_138384.4(MTG1):c.137T>A (p.Leu46Gln)	MTG1 (L46Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398299	NM_138384.4(MTG1):c.145G>C (p.Val49Leu)	MTG1 (V49L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476884	NM_138384.4(MTG1):c.187T>G (p.Ser63Ala)	MTG1 (S63A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456515	NM_138384.4(MTG1):c.191G>C (p.Gly64Ala)	MTG1 (G64A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296614	NM_138384.4(MTG1):c.202C>A (p.Leu68Met)	MTG1 (L68M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214835	NM_138384.4(MTG1):c.209A>G (p.Gln70Arg)	MTG1 (Q70R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214844	NM_138384.4(MTG1):c.433T>C (p.Cys145Arg)	MTG1 (C145R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214847	NM_138384.4(MTG1):c.460G>A (p.Val154Met)	MTG1 (V154M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296616	NM_138384.4(MTG1):c.487C>T (p.Leu163Phe)	MTG1 (L163F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471284	NM_138384.4(MTG1):c.554C>A (p.Ala185Asp)	MTG1 (A185D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 781793	NM_138384.4(MTG1):c.588C>T (p.Pro196=)	MTG1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3214854	NM_138384.4(MTG1):c.589C>A (p.Leu197Met)	MTG1 (L197M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539753	NM_138384.4(MTG1):c.592A>G (p.Met198Val)	MTG1 (M198V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2320032	NM_138384.4(MTG1):c.650G>A (p.Gly217Asp)	MTG1 (G217D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540586	NM_138384.4(MTG1):c.697G>A (p.Glu233Lys)	MTG1 (E233K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214870	NM_138384.4(MTG1):c.706A>G (p.Met236Val)	MTG1 (M236V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465014	NM_138384.4(MTG1):c.714C>G (p.Asp238Glu)	MTG1 (D238E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226652	NM_138384.4(MTG1):c.716A>G (p.Tyr239Cys)	MTG1 (Y239C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2330795	NM_138384.4(MTG1):c.727A>C (p.Thr243Pro)	MTG1 (T243P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2563800	NM_138384.4(MTG1):c.745C>T (p.Arg249Cys)	MTG1 (R249C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214886	NM_138384.4(MTG1):c.757G>A (p.Val253Met)	MTG1 (V253M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2641032	NM_138384.4(MTG1):c.801C>T (p.Arg267=)	MTG1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2314735	NM_138384.4(MTG1):c.836C>T (p.Thr279Met)	MTG1 (T279M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3296615	NM_138384.4(MTG1):c.881T>C (p.Ile294Thr)	MTG1 (I294T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214893	NM_138384.4(MTG1):c.911A>C (p.Asp304Ala)	MTG1 (D304A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553435	NM_138384.4(MTG1):c.964G>A (p.Asp322Asn)	MTG1 (D322N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277463	NM_138384.4(MTG1):c.973C>T (p.Arg325Trp)	MTG1 (R325W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248587	NM_138384.4(MTG1):c.986C>T (p.Pro329Leu)	MTG1 (P329L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251068	NM_138384.4(MTG1):c.994A>C (p.Thr332Pro)	MTG1 (T332P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3214816	NM_138384.4(MTG1):c.1000C>T (p.Pro334Ser)	MTG1 (P334S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 31