"Ambry Genetics"[submitter] AND "LMOD2"[gene] - ClinVar

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Items: 35

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2457647	NM_207163.3(LMOD2):c.40G>A (p.Glu14Lys)	LMOD2 (E14K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3290992	NM_207163.3(LMOD2):c.67G>T (p.Ala23Ser)	LMOD2 (A23S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3290994	NM_207163.3(LMOD2):c.68C>T (p.Ala23Val)	LMOD2 (A23V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2470286	NM_207163.3(LMOD2):c.94G>A (p.Glu32Lys)	LMOD2 (E32K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3119391	NM_207163.3(LMOD2):c.131G>A (p.Arg44His)	LMOD2 (R44H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2287385	NM_207163.3(LMOD2):c.176C>A (p.Thr59Asn)	LMOD2 (T59N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2313596	NM_207163.3(LMOD2):c.251A>G (p.Glu84Gly)	LMOD2 (E84G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2547756	NM_207163.3(LMOD2):c.263A>C (p.Glu88Ala)	LMOD2 (E88A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2278455	NM_207163.3(LMOD2):c.334G>A (p.Val112Ile)	LMOD2 (V112I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2399033	NM_207163.3(LMOD2):c.385G>C (p.Glu129Gln)	LMOD2 (E129Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3119394	NM_207163.3(LMOD2):c.412G>C (p.Glu138Gln)	LMOD2 (E138Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3119395	NM_207163.3(LMOD2):c.491A>C (p.Lys164Thr)	LMOD2 (K164T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3119396	NM_207163.3(LMOD2):c.492G>T (p.Lys164Asn)	LMOD2 (K164N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2379215	NM_207163.3(LMOD2):c.580G>A (p.Gly194Arg)	LMOD2 (G194R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2455225	NM_207163.3(LMOD2):c.691C>T (p.Arg231Cys)	LMOD2 (R231C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2402557	NM_207163.3(LMOD2):c.731C>T (p.Thr244Met)	LMOD2 (T244M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2266094	NM_207163.3(LMOD2):c.757G>A (p.Asp253Asn)	LMOD2 (D253N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3119398	NM_207163.3(LMOD2):c.779T>C (p.Ile260Thr)	LMOD2 (I260T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2231297	NM_207163.3(LMOD2):c.842C>T (p.Thr281Met)	LMOD2 (T281M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2295479	NM_207163.3(LMOD2):c.924C>A (p.His308Gln)	LMOD2 (H308Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2236736	NM_207163.3(LMOD2):c.972G>C (p.Glu324Asp)	LMOD2 (E324D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2402351	NM_207163.3(LMOD2):c.977C>T (p.Thr326Met)	LMOD2 (T326M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2465115	NM_207163.3(LMOD2):c.1034C>T (p.Thr345Met)	LMOD2 (T345M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2228289	NM_207163.3(LMOD2):c.1040T>C (p.Ile347Thr)	LMOD2 (I347T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2529943	NM_207163.3(LMOD2):c.1160C>G (p.Ser387Cys)	LMOD2 (S387C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2623393	NM_207163.3(LMOD2):c.1226C>G (p.Thr409Ser)	LMOD2 (T409S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2618641	NM_207163.3(LMOD2):c.1285C>T (p.Pro429Ser)	LMOD2 (P429S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3290993	NM_207163.3(LMOD2):c.1311G>T (p.Arg437Ser)	LMOD2 (R437S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3290995	NM_207163.3(LMOD2):c.1322C>T (p.Pro441Leu)	LMOD2 (P441L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3119392	NM_207163.3(LMOD2):c.1337C>T (p.Pro446Leu)	LMOD2 (P446L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2284657	NM_207163.3(LMOD2):c.1445G>C (p.Gly482Ala)	LMOD2 (G482A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2384422	NM_207163.3(LMOD2):c.1496C>A (p.Ser499Tyr)	LMOD2 (S499Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2273573	NM_207163.3(LMOD2):c.1538G>A (p.Arg513Gln)	LMOD2 (R513Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2336605	NM_207163.3(LMOD2):c.1583C>T (p.Ala528Val)	LMOD2 (A528V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3119393	NM_207163.3(LMOD2):c.1640G>A (p.Arg547Gln)	LMOD2 (R547Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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Items: 35