"Ambry Genetics"[submitter] AND "MYL9"[gene] - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2479893	NM_006097.5(MYL9):c.134G>A (p.Arg45His)	DLGAP4-AS1, MYL9 (R45H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3159626	NM_006097.5(MYL9):c.213G>C (p.Glu71Asp)	DLGAP4-AS1, MYL9 (E71D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2456943	NM_006097.5(MYL9):c.290C>T (p.Thr97Met)	DLGAP4-AS1, MYL9 (T97M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2379836	NM_006097.5(MYL9):c.298G>A (p.Glu100Lys)	DLGAP4-AS1, MYL9 (E100K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2351120	NM_006097.5(MYL9):c.316G>A (p.Ala106Thr)	DLGAP4-AS1, MYL9 (A106T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2328036	NM_006097.5(MYL9):c.326G>C (p.Cys109Ser)	DLGAP4-AS1, MYL9 (C109S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3297582	NM_006097.5(MYL9):c.331G>A (p.Asp111Asn)	DLGAP4-AS1, MYL9 (D111N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3297581	NM_006097.5(MYL9):c.397C>T (p.Arg133Cys)	DLGAP4-AS1, MYL9 (R79C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3297579	NM_006097.5(MYL9):c.426G>A (p.Met142Ile)	DLGAP4-AS1, MYL9 (M142I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213404	NM_006097.5(MYL9):c.431G>A (p.Arg144Gln)	DLGAP4-AS1, MYL9 (R144Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241405	NM_006097.5(MYL9):c.510A>C (p.Lys170Asn)	DLGAP4-AS1, MYL9 (K116N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2230425	NM_006097.5(MYL9):c.511G>C (p.Asp171His)	DLGAP4-AS1, MYL9 (D171H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance