"Fulgent Genetics, Fulgent Genetics"[submitter] AND "TMEM127"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 241225	NM_017849.4(TMEM127):c.534C>T (p.Tyr178=)	TMEM127	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 463847	NM_017849.4(TMEM127):c.427G>A (p.Val143Ile)	TMEM127 (V143I)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 480799	NM_017849.4(TMEM127):c.426C>T (p.Thr142=)	TMEM127	Single nucleotide variant (synonymous variant)	Hereditary pheochromocytoma-paraganglioma +2 more	GBenign/Likely benign
Select item 337506	NM_017849.4(TMEM127):c.281G>A (p.Arg94Gln)	TMEM127 (R94Q)	Single nucleotide variant (missense variant)	Hereditary pheochromocytoma-paraganglioma +3 more	GConflicting classifications of pathogenicity
Select item 136209	NM_017849.4(TMEM127):c.268G>A (p.Val90Met)	TMEM127 (V90M)	Single nucleotide variant (missense variant)	not specified +4 more	GBenign/Likely benign
Select item 821649	NM_017849.4(TMEM127):c.266C>T (p.Thr89Ile)	TMEM127 (T89I)	Single nucleotide variant (missense variant)	Pheochromocytoma +2 more	GUncertain significance

ClinVar