"ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 221041	NM_000222.3(KIT):c.67+4G>A	KIT	Single nucleotide variant (intron variant)	Gastrointestinal stromal tumor +4 more	GBenign/Likely benign
Select item 134628	NM_000222.3(KIT):c.503C>T (p.Ala168Val)	KIT (A168V)	Single nucleotide variant (missense variant)	not provided +3 more	GConflicting classifications of pathogenicity
Select item 161259	NM_000222.3(KIT):c.532G>A (p.Ala178Thr)	KIT (A178T)	Single nucleotide variant (missense variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 255571	NM_000222.3(KIT):c.2394C>T (p.Ile798=)	KIT	Single nucleotide variant (synonymous variant)	not provided +5 more	GBenign/Likely benign
Select item 221133	NM_000222.3(KIT):c.2805T>A (p.Ile935=)	KIT	Single nucleotide variant (synonymous variant)	Mastocytosis +6 more	GBenign/Likely benign
Select item 348955	NM_000222.3(KIT):c.2847C>T (p.Pro949=)	KIT	Single nucleotide variant (synonymous variant)	Mastocytosis +5 more	GBenign

ClinVar