CREB3L4[gene] and "single gene"[properties] - ClinVar

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Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2279437	NM_001255978.2(CREB3L4):c.123G>C (p.Arg41Ser)	CREB3L4 (R41S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2254412	NM_001255978.2(CREB3L4):c.166C>T (p.Arg56Cys)	CREB3L4 (R56C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3269461	NM_001255978.2(CREB3L4):c.227A>G (p.Asn76Ser)	CREB3L4 (N76S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598337	NM_001255978.2(CREB3L4):c.254C>T (p.Pro85Leu)	CREB3L4 (P85L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2344145	NM_001255978.2(CREB3L4):c.305C>G (p.Pro102Arg)	CREB3L4 (P82R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212088	NM_001255978.2(CREB3L4):c.334C>T (p.Leu112Phe)	CREB3L4 (L92F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524900	NM_001255978.2(CREB3L4):c.676C>T (p.Arg226Cys)	CREB3L4 (R206C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2590251	NM_001255978.2(CREB3L4):c.691G>A (p.Ala231Thr)	CREB3L4 (A231T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2259989	NM_001255978.2(CREB3L4):c.778C>G (p.Gln260Glu)	CREB3L4 (Q240E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2256939	NM_001255978.2(CREB3L4):c.845C>T (p.Thr282Met)	CREB3L4 (T282M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3269460	NM_001255978.2(CREB3L4):c.919C>G (p.Leu307Val)	CREB3L4 (L287V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2612098	NM_001255978.2(CREB3L4):c.948C>G (p.Phe316Leu)	CREB3L4 (F296L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2517545	NM_001255978.2(CREB3L4):c.959C>T (p.Pro320Leu)	CREB3L4 (P300L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2230436	NM_001255978.2(CREB3L4):c.985C>T (p.Pro329Ser)	CREB3L4 (P309S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2485474	NM_001255978.2(CREB3L4):c.1015A>T (p.Thr339Ser)	CREB3L4 (T339S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3269459	NM_001255978.2(CREB3L4):c.1051G>C (p.Val351Leu)	CREB3L4 (V331L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2335192	NM_001255978.2(CREB3L4):c.1084G>A (p.Ala362Thr)	CREB3L4 (A362T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2342150	NM_001255978.2(CREB3L4):c.1120G>A (p.Glu374Lys)	CREB3L4 (E354K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2306108	NM_001255978.2(CREB3L4):c.1145C>T (p.Pro382Leu)	CREB3L4 (P382L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2355913	NM_001255978.2(CREB3L4):c.1150G>A (p.Gly384Arg)	CREB3L4 (G384R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2343731	NM_001255978.2(CREB3L4):c.1150G>T (p.Gly384Trp)	CREB3L4 (G384W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2341636	NM_001255978.2(CREB3L4):c.1165G>A (p.Val389Met)	CREB3L4 (V369M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 22