"Ambry Genetics"[submitter] AND "PLPP2"[gene] - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3215381	NM_003712.4(PLPP2):c.847T>G (p.Tyr283Asp)	PLPP2 (Y227D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528413	NM_003712.4(PLPP2):c.831C>A (p.Asp277Glu)	PLPP2 (D298E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317983	NM_003712.4(PLPP2):c.823G>A (p.Glu275Lys)	PLPP2 (E219K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387699	NM_003712.4(PLPP2):c.703G>C (p.Val235Leu)	PLPP2 (V235L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283368	NM_003712.4(PLPP2):c.692A>T (p.Gln231Leu)	PLPP2 (Q252L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283896	NM_003712.4(PLPP2):c.670G>A (p.Asp224Asn)	PLPP2 (D245N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306804	NM_003712.4(PLPP2):c.661C>T (p.His221Tyr)	PLPP2 (H242Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359548	NM_003712.4(PLPP2):c.577C>T (p.Arg193Trp)	PLPP2 (R193W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532662	NM_003712.4(PLPP2):c.547G>A (p.Val183Met)	PLPP2 (V127M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267247	NM_003712.4(PLPP2):c.526A>G (p.Met176Val)	PLPP2 (M120V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215379	NM_003712.4(PLPP2):c.475G>A (p.Glu159Lys)	PLPP2 (E159K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396161	NM_003712.4(PLPP2):c.445G>A (p.Val149Met)	PLPP2 (V149M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484132	NM_003712.4(PLPP2):c.410G>C (p.Arg137Pro)	PLPP2 (R137P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552990	NM_003712.4(PLPP2):c.359T>C (p.Ile120Thr)	PLPP2 (I120T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3215378	NM_003712.4(PLPP2):c.357G>A (p.Met119Ile)	PLPP2 (M63I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208923	NM_003712.4(PLPP2):c.214G>A (p.Gly72Arg)	PLPP2 (G16R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217409	NM_003712.4(PLPP2):c.169A>G (p.Met57Val)	PLPP2 (M78V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3215377	NM_003712.4(PLPP2):c.158C>T (p.Thr53Ile)	PLPP2 (T74I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3215376	NM_003712.4(PLPP2):c.149A>T (p.Asp50Val)	PLPP2 (D50V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2520574	NM_003712.4(PLPP2):c.143G>A (p.Arg48His)	PLPP2 (R48H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2392519	NM_003712.4(PLPP2):c.142C>T (p.Arg48Cys)	PLPP2 (R69C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2304924	NM_003712.4(PLPP2):c.97A>G (p.Lys33Glu)	PLPP2 (K33E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2456289	NM_003712.4(PLPP2):c.92C>T (p.Pro31Leu)	PLPP2 (P52L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2323886	NM_003712.4(PLPP2):c.77C>T (p.Thr26Met)	PLPP2 (T26M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2599563	NM_003712.4(PLPP2):c.52+259C>T	LOC108281123, PLPP2 (P14L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2528290	NM_003712.4(PLPP2):c.52+246C>T	LOC108281123, PLPP2 (R10W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 26