"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "NR4A2"[gen - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2651440	NC_000002.12:g.156238340T>C	LINC01876, NR4A2	Single nucleotide variant	not provided	GBenign
Select item 331652	NM_006186.4(NR4A2):c.659_661del	NR4A2	Deletion (3 prime UTR variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3067505	NM_006186.4(NR4A2):c.1577A>G (p.Glu526Gly)	NR4A2 (E463G +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 808830	NM_006186.4(NR4A2):c.1494_1497dup (p.Ile500fs)	NR4A2 (I437fs +1 more)	Duplication (frameshift variant)	not provided	GLikely pathogenic
Select item 2651441	NM_006186.4(NR4A2):c.1287C>T (p.Asp429=)	NR4A2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 871822	NM_006186.4(NR4A2):c.825C>A (p.Tyr275Ter)	NR4A2 (Y212* +1 more)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 331661	NM_006186.4(NR4A2):c.732C>A (p.Leu244=)	NR4A2	Single nucleotide variant (synonymous variant)	Parkinson disease, late-onset +2 more	GBenign/Likely benign
Select item 2651442	NM_006186.4(NR4A2):c.717C>T (p.His239=)	NR4A2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 331662	NM_006186.4(NR4A2):c.657T>C (p.Ala219=)	NR4A2	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1684964	NM_006186.4(NR4A2):c.289A>G (p.Met97Val)	NR4A2 (M34V +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 1298829	NM_006186.4(NR4A2):c.79T>C (p.Ser27Pro)	NR4A2 (S27P)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance