"Ambry Genetics"[submitter] AND "PLPP5"[gene] - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2457612	NM_001102559.2(PLPP5):c.773A>C (p.Asp258Ala)	DDHD2, PLPP5 (D258A +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3215396	NM_001102559.2(PLPP5):c.727C>T (p.Pro243Ser)	DDHD2, PLPP5 (P111S +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2383131	NM_001102559.2(PLPP5):c.613G>C (p.Asp205His)	DDHD2, PLPP5 (D205H +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3215395	NM_001102559.2(PLPP5):c.401G>A (p.Cys134Tyr)	PLPP5, DDHD2 (C163Y +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3215394	NM_001102559.2(PLPP5):c.385C>T (p.His129Tyr)	DDHD2, PLPP5 (H158Y +3 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2221412	NM_001102559.2(PLPP5):c.362G>T (p.Arg121Leu)	DDHD2, PLPP5 (R121L +3 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2530644	NM_001102559.2(PLPP5):c.347C>G (p.Pro116Arg)	DDHD2, PLPP5 (P75R +3 more)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2520684	NM_001102559.2(PLPP5):c.298A>C (p.Asn100His)	DDHD2, PLPP5 (N82H +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2350993	NM_001102559.2(PLPP5):c.292G>A (p.Ala98Thr)	DDHD2, PLPP5 (A57T +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2407062	NM_001102559.2(PLPP5):c.286G>C (p.Ala96Pro)	DDHD2, PLPP5 (A125P +4 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3307823	NM_001102559.2(PLPP5):c.251G>C (p.Arg84Thr)	DDHD2, PLPP5 (R113T +3 more)	Single nucleotide variant (missense variant +3 more)	not specified	GLikely benign
Select item 2223911	NM_001102559.2(PLPP5):c.59T>A (p.Leu20Gln)	DDHD2, LOC130000223 +1 more (L20Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2281325	NM_001102559.2(PLPP5):c.22G>T (p.Val8Leu)	DDHD2, LOC130000223 +1 more (V8L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2308843	NM_001102559.2(PLPP5):c.14C>T (p.Ala5Val)	DDHD2, LOC130000223 +1 more (A5V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance