"Ambry Genetics"[submitter] AND "SMYD2"[gene] - ClinVar

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Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2262417	NM_020197.3(SMYD2):c.29A>T (p.Glu10Val)	LOC129932500, SMYD2 (E10V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166794	NM_020197.3(SMYD2):c.32G>C (p.Arg11Pro)	LOC129932500, SMYD2 (R11P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240190	NM_020197.3(SMYD2):c.116A>G (p.Tyr39Cys)	LOC129932500, SMYD2 (Y39C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312413	NM_020197.3(SMYD2):c.142C>T (p.Arg48Trp)	SMYD2 (R48W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552120	NM_020197.3(SMYD2):c.253A>G (p.Met85Val)	SMYD2 (M85V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351130	NM_020197.3(SMYD2):c.293A>G (p.Glu98Gly)	SMYD2 (E98G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166793	NM_020197.3(SMYD2):c.295A>C (p.Asn99His)	SMYD2 (N99H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341897	NM_020197.3(SMYD2):c.305C>T (p.Pro102Leu)	SMYD2 (P102L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166795	NM_020197.3(SMYD2):c.407C>T (p.Ser136Leu)	SMYD2 (S136L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271927	NM_020197.3(SMYD2):c.496T>A (p.Phe166Ile)	SMYD2 (F166I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3321074	NM_020197.3(SMYD2):c.514C>T (p.Leu172Phe)	SMYD2 (L172F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235804	NM_020197.3(SMYD2):c.568G>A (p.Glu190Lys)	SMYD2 (E190K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517891	NM_020197.3(SMYD2):c.590C>T (p.Ala197Val)	SMYD2 (A197V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253423	NM_020197.3(SMYD2):c.619C>G (p.His207Asp)	SMYD2 (H207D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467903	NM_020197.3(SMYD2):c.695C>G (p.Pro232Arg)	SMYD2 (P232R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206103	NM_020197.3(SMYD2):c.850G>A (p.Asp284Asn)	SMYD2 (D284N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359275	NM_020197.3(SMYD2):c.875G>A (p.Arg292Gln)	SMYD2 (R292Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166796	NM_020197.3(SMYD2):c.926A>G (p.Lys309Arg)	SMYD2 (K309R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2314429	NM_020197.3(SMYD2):c.964G>A (p.Glu322Lys)	SMYD2 (E322K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166791	NM_020197.3(SMYD2):c.1128G>C (p.Leu376Phe)	SMYD2 (L376F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3166792	NM_020197.3(SMYD2):c.1265A>C (p.Tyr422Ser)	SMYD2 (Y422S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520785	NM_020197.3(SMYD2):c.1273G>A (p.Glu425Lys)	SMYD2 (E425K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 22