"PreventionGenetics, part of Exact Sciences"[submitter] AND "USP15"[ge - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3060061	NM_001252078.2(USP15):c.246C>T (p.His82=)	USP15	Single nucleotide variant (synonymous variant +2 more)	USP15-related disorder	GBenign
Select item 3042654	NM_001252078.2(USP15):c.801A>G (p.Ser267=)	USP15	Single nucleotide variant (synonymous variant +2 more)	USP15-related disorder	GLikely benign
Select item 2360631	NM_001252078.2(USP15):c.1310T>C (p.Ile437Thr)	USP15 (I104T +4 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3033240	NM_001252078.2(USP15):c.1371A>G (p.Thr457=)	USP15	Single nucleotide variant (synonymous variant +1 more)	USP15-related disorder	GLikely benign
Select item 3060073	NM_001252078.2(USP15):c.1455A>G (p.Pro485=)	USP15	Single nucleotide variant (synonymous variant +1 more)	USP15-related disorder	GBenign
Select item 2632097	NM_001252078.2(USP15):c.1506A>G (p.Ile502Met)	USP15 (I169M +4 more)	Single nucleotide variant (missense variant +1 more)	USP15-related disorder	GUncertain significance
Select item 3050545	NM_001252078.2(USP15):c.1572T>C (p.Asp524=)	USP15	Single nucleotide variant (synonymous variant +1 more)	USP15-related disorder	GLikely benign
Select item 3045839	NM_001252078.2(USP15):c.1602C>T (p.Phe534=)	USP15	Single nucleotide variant (synonymous variant +1 more)	USP15-related disorder	GLikely benign
Select item 2360632	NM_001252078.2(USP15):c.2061T>G (p.Asp687Glu)	USP15 (D354E +4 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3059803	NM_001252078.2(USP15):c.2301T>C (p.Ala767=)	USP15	Single nucleotide variant (synonymous variant +1 more)	USP15-related disorder	GBenign