"Ambry Genetics"[submitter] AND "DEPDC4"[gene] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2396932	NM_001364818.2(DEPDC4):c.676C>A (p.Pro226Thr)	DEPDC4 (P226T +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3081743	NM_001364818.2(DEPDC4):c.611T>C (p.Ile204Thr)	DEPDC4 (I137T +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2337064	NM_001364818.2(DEPDC4):c.599G>T (p.Gly200Val)	DEPDC4 (G133V +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2517242	NM_001364818.2(DEPDC4):c.587C>T (p.Ala196Val)	DEPDC4 (A196V +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2316909	NM_001364818.2(DEPDC4):c.418A>G (p.Lys140Glu)	DEPDC4 (K73E +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2251923	NM_001364818.2(DEPDC4):c.414G>T (p.Met138Ile)	DEPDC4 (M71I +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2308999	NM_001364818.2(DEPDC4):c.375A>C (p.Gln125His)	DEPDC4 (Q125H +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2549496	NM_001364818.2(DEPDC4):c.355A>G (p.Lys119Glu)	DEPDC4 (K119E)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3081741	NM_001364818.2(DEPDC4):c.314T>G (p.Met105Arg)	DEPDC4 (M105R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2328451	NM_001364818.2(DEPDC4):c.262A>G (p.Lys88Glu)	DEPDC4 (K88E)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2363736	NM_001364818.2(DEPDC4):c.194A>C (p.Asp65Ala)	DEPDC4 (D65A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3271630	NM_001364818.2(DEPDC4):c.169C>A (p.Pro57Thr)	DEPDC4 (P57T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2260851	NM_001364818.2(DEPDC4):c.154A>G (p.Thr52Ala)	DEPDC4, LOC130008539 (T52A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2228351	NM_001364818.2(DEPDC4):c.85C>T (p.Leu29Phe)	DEPDC4, LOC130008539 (L29F)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3271631	NM_001364818.2(DEPDC4):c.50C>T (p.Thr17Ile)	DEPDC4 (T17I)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3081742	NM_001364818.2(DEPDC4):c.37G>C (p.Ala13Pro)	DEPDC4 (A13P)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3081740	NM_001364818.2(DEPDC4):c.22G>C (p.Ala8Pro)	DEPDC4 (A8P)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3081739	NM_001364818.2(DEPDC4):c.17A>G (p.Glu6Gly)	DEPDC4 (E6G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance