SCAMP4[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2279143	NM_079834.4(SCAMP4):c.119T>G (p.Ile40Ser)	SCAMP4 (I40S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2392065	NM_079834.4(SCAMP4):c.166A>G (p.Ile56Val)	SCAMP4 (I56V +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2375206	NM_079834.4(SCAMP4):c.214G>A (p.Gly72Ser)	SCAMP4 (G72S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2648951	NM_079834.4(SCAMP4):c.246G>A (p.Thr82=)	SCAMP4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2306126	NM_079834.4(SCAMP4):c.266G>C (p.Trp89Ser)	SCAMP4 (W45S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278200	NM_079834.4(SCAMP4):c.412A>G (p.Ile138Val)	SCAMP4 (I94V +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2404993	NM_079834.4(SCAMP4):c.434C>T (p.Pro145Leu)	SCAMP4 (P111L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241899	NM_079834.4(SCAMP4):c.478G>A (p.Val160Met)	SCAMP4 (V126M +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2648952	NM_079834.4(SCAMP4):c.482C>T (p.Ser161Leu)	SCAMP4 (S117L +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2365901	NM_079834.4(SCAMP4):c.502G>A (p.Ala168Thr)	SCAMP4 (A134T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158217	NM_079834.4(SCAMP4):c.508A>G (p.Met170Val)	SCAMP4 (M126V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470981	NM_079834.4(SCAMP4):c.563C>T (p.Thr188Met)	SCAMP4 (T144M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158218	NM_079834.4(SCAMP4):c.578G>A (p.Gly193Asp)	SCAMP4 (G193D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158219	NM_079834.4(SCAMP4):c.581C>T (p.Thr194Ile)	SCAMP4 (T150I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607653	NM_079834.4(SCAMP4):c.604G>C (p.Glu202Gln)	SCAMP4 (E168Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242448	NM_079834.4(SCAMP4):c.608C>T (p.Ala203Val)	SCAMP4 (A203V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158220	NM_079834.4(SCAMP4):c.653C>G (p.Thr218Ser)	SCAMP4 (T174S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3158221	NM_079834.4(SCAMP4):c.655G>A (p.Val219Met)	SCAMP4 (V185M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271516	NM_079834.4(SCAMP4):c.662G>T (p.Ser221Ile)	SCAMP4 (S187I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance