"Ambry Genetics"[submitter] AND "MYC"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2286886	NM_002467.6(MYC):c.409G>C (p.Glu137Gln)	MYC (E137Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3297249	NM_002467.6(MYC):c.544G>A (p.Gly182Ser)	MYC (G181S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510151	NM_002467.6(MYC):c.671C>T (p.Ala224Val)	MYC (A223V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468497	NM_002467.6(MYC):c.909C>G (p.Ser303Arg)	MYC (S302R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3154445	NM_002467.6(MYC):c.1228A>G (p.Ile410Val)	MYC (I410V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3154448	NM_002467.6(MYC):c.1297G>C (p.Asp433His)	MYC (D432H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar