C1458155[trait identifier] AND "Genomic Center, National Cancer Instit - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1706623	NM_002228.4(JUN):c.659del (p.Pro220fs)	JUN, LOC129930620 (P220fs)	Deletion (frameshift variant)	Breast neoplasm	GPathogenic
Select item 1706624	NM_001826.3(CKS1B):c.33del (p.Lys11fs)	CKS1B, SHC1 (K11fs)	Deletion (frameshift variant +1 more)	Breast neoplasm	GPathogenic
Select item 1706625	NM_001826.3(CKS1B):c.51del (p.Phe17fs)	CKS1B, LOC129931529 +1 more (F17fs)	Deletion (frameshift variant +1 more)	Breast neoplasm	GPathogenic
Select item 1706620	NM_000586.4(IL2):c.433del (p.Cys145fs)	IL2 (C145fs)	Deletion (frameshift variant)	Breast neoplasm	GPathogenic
Select item 1706621	NM_000586.4(IL2):c.134del (p.Ile44_Leu45insTer)	IL2	Deletion (nonsense)	Breast neoplasm	GPathogenic
Select item 1706622	NM_002185.5(IL7R):c.470del (p.Lys157fs)	IL7R (K157fs)	Deletion (frameshift variant +1 more)	Breast neoplasm	GPathogenic

ClinVar