Related gene-specific medical variations for Gene (Select 8611) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3215375	NM_003711.4(PLPP1):c.827A>G (p.Asn276Ser)	MTREX, PLPP1 (N276S +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3215372	NM_003711.4(PLPP1):c.43C>A (p.Leu15Ile)	LOC129993899, PLPP1 (L15I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2595172	NM_003711.4(PLPP1):c.826A>T (p.Asn276Tyr)	MTREX, PLPP1 (N276Y +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2457703	NM_003711.4(PLPP1):c.836C>T (p.Pro279Leu)	MTREX, PLPP1 (P280L +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2263332	NM_003711.4(PLPP1):c.54G>C (p.Leu18Phe)	LOC129993899, PLPP1 (L18F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2216760	NM_003711.4(PLPP1):c.781G>C (p.Glu261Gln)	MTREX, PLPP1 (E262Q +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance

ClinVar