Related gene-specific medical variations for Gene (Select 23082) - ClinVar

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Links from Gene

Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3217969	NM_015062.5(PPRC1):c.889G>A (p.Ala297Thr)	LOC126861022, PPRC1 (A177T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3217968	NM_015062.5(PPRC1):c.77G>C (p.Gly26Ala)	LOC130004586, PPRC1 (G26A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3217967	NM_015062.5(PPRC1):c.721C>G (p.Gln241Glu)	LOC126861022, PPRC1 (Q121E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3217966	NM_015062.5(PPRC1):c.515G>A (p.Arg172Gln)	LOC126861022, PPRC1 (R52Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3217953	NM_015062.5(PPRC1):c.35C>T (p.Ala12Val)	LOC130004585, PPRC1 (A12V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3043437	NM_015062.5(PPRC1):c.19C>A (p.Arg7=)	LOC130004585, PPRC1	Single nucleotide variant (synonymous variant +1 more)	PPRC1-related disorder	GLikely benign
Select item 3033278	NM_015062.5(PPRC1):c.859G>C (p.Ala287Pro)	LOC126861022, PPRC1 (A167P +1 more)	Single nucleotide variant (missense variant)	PPRC1-related disorder	GBenign
Select item 2689822	NM_015062.5(PPRC1):c.1825C>T (p.Pro609Ser)	PPRC1 (P489S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2640778	NM_015062.5(PPRC1):c.624C>T (p.Asp208=)	LOC126861022, PPRC1	Single nucleotide variant (synonymous variant)	PPRC1-related disorder +1 more	GBenign/Likely benign
Select item 2640776	NM_015062.5(PPRC1):c.24A>G (p.Arg8=)	LOC130004585, PPRC1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2561980	NM_015062.5(PPRC1):c.47G>A (p.Ser16Asn)	LOC130004585, PPRC1 (S16N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2548557	NM_015062.5(PPRC1):c.508C>T (p.Leu170Phe)	LOC126861022, PPRC1 (L50F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545222	NM_015062.5(PPRC1):c.417T>A (p.Asp139Glu)	LOC126861022, PPRC1 (D139E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2543725	NM_015062.5(PPRC1):c.49G>C (p.Gly17Arg)	LOC130004585, PPRC1 (G17R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2537755	NM_015062.5(PPRC1):c.827T>G (p.Met276Arg)	LOC126861022, PPRC1 (M276R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468322	NM_015062.5(PPRC1):c.133G>A (p.Ala45Thr)	LOC130004586, PPRC1 (A45T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2467549	NM_015062.5(PPRC1):c.566G>A (p.Ser189Asn)	LOC126861022, PPRC1 (S69N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455915	NM_015062.5(PPRC1):c.14G>T (p.Arg5Leu)	LOC130004585, PPRC1 (R5L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2379759	NM_015062.5(PPRC1):c.7G>T (p.Ala3Ser)	LOC130004585, PPRC1 (A3S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2335504	NM_015062.5(PPRC1):c.784G>A (p.Gly262Arg)	LOC126861022, PPRC1 (G142R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316877	NM_015062.5(PPRC1):c.395C>T (p.Thr132Met)	LOC126861022, PPRC1 (T132M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2295785	NM_015062.5(PPRC1):c.95G>T (p.Trp32Leu)	LOC130004586, PPRC1 (W32L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2295784	NM_015062.5(PPRC1):c.61C>G (p.Pro21Ala)	LOC130004585, LOC130004586 +1 more (P21A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2254828	NM_015062.5(PPRC1):c.125C>T (p.Thr42Ile)	LOC130004586, PPRC1 (T42I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 161691	NM_015062.5(PPRC1):c.904A>G (p.Ile302Val)	LOC126861022, PPRC1 (I302V +1 more)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance

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Links from Gene

Items: 25