List of variants in gene PTPRC reported by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_002838.5(PTPRC):c.577A>G (p.Thr193Ala)	rs4915154	0.01733
NM_002838.5(PTPRC):c.1268C>T (p.Thr423Ile)	rs6696162	0.00748
NM_002838.5(PTPRC):c.1568A>T (p.Glu523Val)	rs116464756	0.00241
NM_002838.5(PTPRC):c.3402C>T (p.Pro1134=)	rs61757805	0.00238
NM_002838.5(PTPRC):c.3670G>A (p.Val1224Ile)	rs150672767	0.00156
NM_002838.5(PTPRC):c.1297G>A (p.Asp433Asn)	rs140403368	0.00103
NM_002838.5(PTPRC):c.982A>G (p.Ile328Val)	rs41314039	0.00063
NM_002838.5(PTPRC):c.2320C>T (p.Arg774Trp)	rs200672643	0.00004
NM_002838.5(PTPRC):c.1818G>A (p.Lys606=)	rs575318196	0.00003
NM_002838.5(PTPRC):c.177C>G (p.Pro59=)	rs17612648
NM_002838.5(PTPRC):c.3465A>C (p.Glu1155Asp)	rs1558041011
NM_002838.5(PTPRC):c.566T>A (p.Ile189Asn)	rs201715157
NM_002838.5(PTPRC):c.692A>G (p.Lys231Arg)	rs1553239146
NM_002838.5(PTPRC):c.933T>C (p.Cys311=)	rs766607810

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