"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "PTPRO"[gen - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2642760	NM_030667.3(PTPRO):c.712A>T (p.Asn238Tyr)	PTPRO (N238Y)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2642761	NM_030667.3(PTPRO):c.1872T>C (p.Ser624=)	PTPRO	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642762	NM_030667.3(PTPRO):c.3297A>G (p.Ala1099=)	PTPRO	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1711362	GRCh37/hg19 12p13.2-12.1(chr12:10853887-24103810)x1	TAS2R43, YBX3 +85 more	Copy number loss	not provided	GPathogenic

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