"Ambry Genetics"[submitter] AND "EIF3K"[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3087972	NM_013234.4(EIF3K):c.7A>G (p.Met3Val)	EIF3K (M3V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3087966	NM_013234.4(EIF3K):c.32T>G (p.Val11Gly)	EIF3K (V11G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2457834	NM_013234.4(EIF3K):c.199G>A (p.Ala67Thr)	EIF3K (A67T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2340214	NM_013234.4(EIF3K):c.316G>A (p.Gly106Arg)	EIF3K (G19R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3087967	NM_013234.4(EIF3K):c.346G>T (p.Ala116Ser)	EIF3K (A29S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3087968	NM_013234.4(EIF3K):c.403G>A (p.Glu135Lys)	EIF3K, LOC126862903 (E135K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312279	NM_013234.4(EIF3K):c.410C>G (p.Ser137Cys)	EIF3K, LOC126862903 (S137C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3087969	NM_013234.4(EIF3K):c.463C>T (p.Arg155Cys)	EIF3K, LOC126862903 (R68C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2391248	NM_013234.4(EIF3K):c.464G>A (p.Arg155His)	EIF3K, LOC126862903 (R68H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2489703	NM_013234.4(EIF3K):c.484C>T (p.Leu162Phe)	EIF3K, LOC126862903 (L162F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3087971	NM_013234.4(EIF3K):c.584G>A (p.Ser195Asn)	EIF3K (S108N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance