"Ambry Genetics"[submitter] AND "EIF3D"[gene] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2600905	NM_003753.4(EIF3D):c.1484T>C (p.Ile495Thr)	EIF3D (I495T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3087951	NM_003753.4(EIF3D):c.1474C>T (p.Arg492Cys)	EIF3D (R492C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3275002	NM_003753.4(EIF3D):c.1132G>A (p.Asp378Asn)	EIF3D (D378N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2406384	NM_003753.4(EIF3D):c.1019C>G (p.Pro340Arg)	EIF3D (P340R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3275004	NM_003753.4(EIF3D):c.665G>A (p.Arg222His)	EIF3D (R222H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3275005	NM_003753.4(EIF3D):c.583T>C (p.Cys195Arg)	EIF3D (C195R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2404567	NM_003753.4(EIF3D):c.446A>G (p.Lys149Arg)	EIF3D (K149R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3275003	NM_003753.4(EIF3D):c.265C>G (p.Gln89Glu)	EIF3D (Q89E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3087952	NM_003753.4(EIF3D):c.262A>C (p.Thr88Pro)	EIF3D (T88P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2617221	NM_003753.4(EIF3D):c.77G>A (p.Arg26Gln)	EIF3D (R26Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance