"Ambry Genetics"[submitter] AND "CREB5"[gene] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3077335	NM_182898.4(CREB5):c.76C>T (p.Arg26Cys)	CREB5 (R19C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2458270	NM_182898.4(CREB5):c.299C>T (p.Ser100Leu)	CREB5 (S100L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598943	NM_182898.4(CREB5):c.329C>T (p.Thr110Met)	CREB5 (T110M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404672	NM_182898.4(CREB5):c.337G>A (p.Gly113Arg)	CREB5 (G80R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550403	NM_182898.4(CREB5):c.365T>A (p.Leu122Gln)	CREB5 (L122Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473786	NM_182898.4(CREB5):c.372C>G (p.Asn124Lys)	CREB5 (N91K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077332	NM_182898.4(CREB5):c.413C>T (p.Pro138Leu)	CREB5 (P105L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077333	NM_182898.4(CREB5):c.421A>T (p.Ser141Cys)	CREB5 (S141C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077334	NM_182898.4(CREB5):c.454C>T (p.Arg152Cys)	CREB5 (R152C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393628	NM_182898.4(CREB5):c.599G>A (p.Arg200Gln)	CREB5 (R167Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482603	NM_182898.4(CREB5):c.662C>A (p.Ala221Asp)	CREB5 (A214D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617814	NM_182898.4(CREB5):c.682A>G (p.Met228Val)	CREB5 (M228V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2461683	NM_182898.4(CREB5):c.754A>G (p.Met252Val)	CREB5 (M113V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3269463	NM_182898.4(CREB5):c.767G>T (p.Gly256Val)	CREB5 (G117V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382228	NM_182898.4(CREB5):c.785T>C (p.Met262Thr)	CREB5 (M255T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524105	NM_182898.4(CREB5):c.794G>A (p.Arg265Gln)	CREB5 (R126Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077336	NM_182898.4(CREB5):c.833C>T (p.Pro278Leu)	CREB5 (P139L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077337	NM_182898.4(CREB5):c.890C>T (p.Pro297Leu)	CREB5 (P158L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409882	NM_182898.4(CREB5):c.907C>A (p.Pro303Thr)	CREB5 (P270T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2472619	NM_182898.4(CREB5):c.1090G>T (p.Gly364Trp)	CREB5 (G331W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334923	NM_182898.4(CREB5):c.1097G>T (p.Arg366Leu)	CREB5 (R366L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3269462	NM_182898.4(CREB5):c.1124A>G (p.Asp375Gly)	CREB5 (D342G +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077329	NM_182898.4(CREB5):c.1192G>T (p.Val398Phe)	CREB5 (V259F +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077330	NM_182898.4(CREB5):c.1295A>G (p.Lys432Arg)	CREB5 (K432R +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3077331	NM_182898.4(CREB5):c.1462G>A (p.Val488Met)	CREB5 (V455M +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 25