ClinVar for MedGen (Select 18279) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 625198	t(8;9)(q24.22;q34.13)	TMEM71, TSC1	Translocation	Neoplasm of the pancreas	GPathogenic
Select item 625197	t(X;8)(p22.13;q12.1)	BEND2, CHD7	Translocation	Neoplasm of the pancreas	GUncertain significance
Select item 376707	NM_178170.3(NEK8):c.589G>C (p.Ala197Pro)	NEK8 (A197P)	Single nucleotide variant (missense variant)	Neoplasm of the pancreas	GLikely pathogenic
Select item 376702	NM_001352389.2(STK33):c.969T>G (p.Phe323Leu)	STK33 (F136L +2 more)	Single nucleotide variant (missense variant)	Neoplasm of the pancreas	GLikely pathogenic
Select item 376700	NM_003318.5(TTK):c.2089G>T (p.Asp697Tyr)	TTK (D696Y +1 more)	Single nucleotide variant (missense variant)	Neoplasm of the pancreas	GLikely pathogenic
Select item 376187	NM_000455.5(STK11):c.582C>G (p.Asp194Glu)	STK11 (D194E)	Single nucleotide variant (missense variant)	Neoplasm of the pancreas	GLikely pathogenic
Select item 185384	NM_000455.5(STK11):c.582C>A (p.Asp194Glu)	STK11 (D194E)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +1 more	GLikely pathogenic

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