C1970712[trait identifier] AND "KCCC/NGS Laboratory, Kuwait Cancer Con - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 13909	NM_020975.6(RET):c.1901G>A (p.Cys634Tyr)	RET (C634Y +14 more)	Single nucleotide variant (missense variant)	not provided +5 more	GPathogenic
Select item 13951	NM_020975.6(RET):c.2671T>G (p.Ser891Ala)	RET (S891A +17 more)	Single nucleotide variant (missense variant)	not provided +10 more	GPathogenic
Select item 307658	NM_004064.5(CDKN1B):c.-79T>C	CDKN1B	Single nucleotide variant (5 prime UTR variant)	Multiple endocrine neoplasia type 4 +1 more	GBenign
Select item 239617	NM_004064.5(CDKN1B):c.165G>A (p.Ala55=)	CDKN1B	Single nucleotide variant (synonymous variant)	Multiple endocrine neoplasia type 4 +2 more	GBenign
Select item 259226	NM_004064.5(CDKN1B):c.326T>G (p.Val109Gly)	CDKN1B (V109G)	Single nucleotide variant (missense variant)	Multiple endocrine neoplasia type 4 +3 more	GBenign
Select item 239622	NM_004064.5(CDKN1B):c.426G>A (p.Thr142=)	CDKN1B	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +3 more	GBenign/Likely benign
Select item 469030	NM_004064.5(CDKN1B):c.543C>G (p.Ala181=)	CDKN1B	Single nucleotide variant (synonymous variant)	CDKN1B-related condition +2 more	GBenign/Likely benign
Select item 412889	NM_004064.5(CDKN1B):c.577C>T (p.Leu193Phe)	CDKN1B (L193F)	Single nucleotide variant (missense variant)	not specified +3 more	GBenign/Likely benign

ClinVar