"Ambry Genetics"[submitter] AND "JUNB"[gene] - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3112560	NM_002229.3(JUNB):c.26T>C (p.Phe9Ser)	HOOK2, JUNB +1 more (F9S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2529796	NM_002229.3(JUNB):c.39C>A (p.Asp13Glu)	HOOK2, JUNB (D13E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3287280	NM_002229.3(JUNB):c.164C>A (p.Ala55Asp)	HOOK2, JUNB (A55D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2378182	NM_002229.3(JUNB):c.200G>C (p.Ser67Thr)	HOOK2, JUNB (S67T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3112559	NM_002229.3(JUNB):c.238C>T (p.Leu80Phe)	HOOK2, JUNB (L80F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2547032	NM_002229.3(JUNB):c.454G>T (p.Val152Leu)	HOOK2, JUNB +1 more (V152L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3287278	NM_002229.3(JUNB):c.481G>A (p.Ala161Thr)	HOOK2, JUNB +1 more (A161T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3287281	NM_002229.3(JUNB):c.482C>T (p.Ala161Val)	HOOK2, JUNB +1 more (A161V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3287277	NM_002229.3(JUNB):c.493C>G (p.Pro165Ala)	HOOK2, JUNB +1 more (P165A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3287279	NM_002229.3(JUNB):c.505C>T (p.Pro169Ser)	HOOK2, JUNB +1 more (P169S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2622294	NM_002229.3(JUNB):c.508G>A (p.Gly170Arg)	HOOK2, JUNB +1 more (G170R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3287276	NM_002229.3(JUNB):c.661C>T (p.Pro221Ser)	JUNB (P221S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296704	NM_002229.3(JUNB):c.679C>T (p.Pro227Ser)	JUNB (P227S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291776	NM_002229.3(JUNB):c.985A>C (p.Met329Leu)	JUNB (M329L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance