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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 636359	NM_002838.5(PTPRC):c.190G>A (p.Glu64Lys)	PTPRC (E64K)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 636483	NM_002838.5(PTPRC):c.421G>C (p.Gly141Arg)	PTPRC (G141R)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GUncertain significance
Select item 636414	NM_002838.5(PTPRC):c.583+1G>A	PTPRC	Single nucleotide variant (splice donor variant +1 more)	not provided +1 more	GLikely pathogenic

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