"Baylor Genetics"[submitter] AND "PTPRC"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 533066	NM_002838.5(PTPRC):c.985G>A (p.Glu329Lys)	PTPRC (E329K +1 more)	Single nucleotide variant (missense variant)	Immunodeficiency 104	GUncertain significance
Select item 1032851	NM_002838.5(PTPRC):c.1084G>A (p.Glu362Lys)	PTPRC (E362K +1 more)	Single nucleotide variant (missense variant)	Immunodeficiency 104	GUncertain significance
Select item 626155	NM_002838.5(PTPRC):c.2142+7A>G	PTPRC	Single nucleotide variant (intron variant)	Immunodeficiency 105 +1 more	GConflicting classifications of pathogenicity
Select item 1032852	NM_002838.5(PTPRC):c.2885T>C (p.Ile962Thr)	PTPRC (I801T +1 more)	Single nucleotide variant (missense variant)	Immunodeficiency 104	GUncertain significance
Select item 190992	NM_002838.5(PTPRC):c.3545T>C (p.Leu1182Ser)	PTPRC (L1182S +1 more)	Single nucleotide variant (missense variant)	Immunodeficiency 104 +4 more	GConflicting classifications of pathogenicity
Select item 1029484	NM_002838.5(PTPRC):c.3832G>C (p.Ala1278Pro)	PTPRC (A1278P +1 more)	Single nucleotide variant (missense variant)	Immunodeficiency 104	GUncertain significance

ClinVar