"Fulgent Genetics, Fulgent Genetics"[submitter] AND "MYCN"[gene] - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 516655	NM_005378.6(MYCN):c.18G>A (p.Thr6=)	MYCN, MYCNOS (V98I)	Single nucleotide variant (synonymous variant +2 more)	not provided +2 more	GLikely benign
Select item 517759	NM_005378.6(MYCN):c.69G>T (p.Ser23=)	MYCN, MYCNOS	Single nucleotide variant (synonymous variant +2 more)	Feingold syndrome type 1 +1 more	GBenign/Likely benign
Select item 703188	NM_005378.6(MYCN):c.279G>A (p.Glu93=)	MYCNOS, MYCN	Single nucleotide variant (non-coding transcript variant +3 more)	not provided +1 more	GLikely benign
Select item 517711	NM_005378.6(MYCN):c.429C>T (p.Ala143=)	MYCN	Single nucleotide variant (synonymous variant +2 more)	Feingold syndrome type 1 +2 more	GLikely benign
Select item 1564664	NM_005378.6(MYCN):c.612C>T (p.Pro204=)	MYCN	Single nucleotide variant (synonymous variant +2 more)	Feingold syndrome type 1 +1 more	GLikely benign
Select item 1224362	NM_005378.6(MYCN):c.718G>A (p.Gly240Ser)	MYCN (G240S)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GUncertain significance
Select item 196409	NM_005378.6(MYCN):c.801_809del	MYCN	Microsatellite	Feingold syndrome type 1 +1 more	GUncertain significance
Select item 1684292	NM_005378.6(MYCN):c.854G>T (p.Arg285Leu)	MYCN (R285L +1 more)	Single nucleotide variant (missense variant +1 more)	Feingold syndrome type 1	GUncertain significance
Select item 702007	NM_005378.6(MYCN):c.1062G>A (p.Ala354=)	MYCN	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 702365	NM_005378.6(MYCN):c.1380C>T (p.His460=)	MYCN	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign