"Ambry Genetics"[submitter] AND "LOC126806207"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2283297	NM_005400.3(PRKCE):c.1081A>G (p.Asn361Asp)	LOC126806207, PRKCE (N361D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252173	NM_005400.3(PRKCE):c.1094A>C (p.Lys365Thr)	LOC126806207, PRKCE (K365T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336681	NM_005400.3(PRKCE):c.1106T>A (p.Phe369Tyr)	LOC126806207, PRKCE (F369Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253497	NM_005400.3(PRKCE):c.1151G>C (p.Gly384Ala)	LOC126806207, PRKCE (G384A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511406	NM_005400.3(PRKCE):c.1166C>G (p.Pro389Arg)	LOC126806207, PRKCE (P389R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484220	NM_005400.3(PRKCE):c.1204C>T (p.Arg402Cys)	LOC126806207, PRKCE (R402C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar