Related gene-specific medical variations for Gene (Select 1051) - ClinVar

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Links from Gene

Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3265691	NM_005194.4(CEBPB):c.505C>T (p.Pro169Ser)	CEBPB, CEBPB-AS1 +1 more (P169S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3265690	NM_005194.4(CEBPB):c.275C>G (p.Thr92Arg)	CEBPB, CEBPB-AS1 +1 more (T92R +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3265689	NM_005194.4(CEBPB):c.752G>A (p.Gly251Glu)	CEBPB, CEBPB-AS1 (G251E +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3265688	NM_005194.4(CEBPB):c.439G>C (p.Ala147Pro)	CEBPB, CEBPB-AS1 +1 more (A147P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141862	NM_005194.4(CEBPB):c.43C>T (p.Pro15Ser)	CEBPB, CEBPB-AS1 (P15S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3141861	NM_005194.4(CEBPB):c.373G>A (p.Asp125Asn)	CEBPB, CEBPB-AS1 +1 more (D102N +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3141860	NM_005194.4(CEBPB):c.159A>C (p.Arg53Ser)	CEBPB, CEBPB-AS1 (R30S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141859	NM_005194.4(CEBPB):c.115G>A (p.Ala39Thr)	CEBPB, CEBPB-AS1 (A16T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2681713	NM_005194.4(CEBPB):c.842ACA[1] (p.Asn282del)	CEBPB, CEBPB-AS1 (N259del +2 more)	Microsatellite (non-coding transcript variant +1 more)	EBV-positive nodal T- and NK-cell lymphoma	GLikely benign
Select item 2615844	NM_005194.4(CEBPB):c.317C>A (p.Pro106His)	CEBPB, CEBPB-AS1 +1 more (P106H +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2612479	NM_005194.4(CEBPB):c.722C>T (p.Ala241Val)	CEBPB, CEBPB-AS1 (A218V +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2514064	NM_005194.4(CEBPB):c.749C>T (p.Ala250Val)	CEBPB, CEBPB-AS1 (A52V +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2484815	NM_005194.4(CEBPB):c.374A>G (p.Asp125Gly)	CEBPB, CEBPB-AS1 +1 more (D102G +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2471607	NM_005194.4(CEBPB):c.258G>C (p.Gln86His)	CEBPB, CEBPB-AS1 +1 more (Q63H +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2380191	NM_005194.4(CEBPB):c.284A>C (p.Asp95Ala)	CEBPB, CEBPB-AS1 +1 more (D72A +1 more)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2360127	NM_005194.4(CEBPB):c.506C>T (p.Pro169Leu)	CEBPB, CEBPB-AS1 +1 more (P169L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2359687	NM_005194.4(CEBPB):c.146C>T (p.Pro49Leu)	CEBPB, CEBPB-AS1 (P26L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2325958	NM_005194.4(CEBPB):c.761C>G (p.Pro254Arg)	CEBPB, CEBPB-AS1 (P231R +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2256637	NM_005194.4(CEBPB):c.578C>G (p.Pro193Arg)	CEBPB, CEBPB-AS1 +1 more (P170R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2249608	NM_005194.4(CEBPB):c.493C>G (p.Pro165Ala)	CEBPB, CEBPB-AS1 +1 more (P142A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2212317	NM_005194.4(CEBPB):c.893A>G (p.Glu298Gly)	CEBPB, CEBPB-AS1 (E100G +2 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 744842	NM_005194.4(CEBPB):c.45G>A (p.Pro15=)	CEBPB, CEBPB-AS1	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GLikely benign

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Links from Gene

Items: 22