"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "WASF1"[gen - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2656837	NM_003931.3(WASF1):c.1398T>G (p.His466Gln)	WASF1 (H466Q)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2656838	NM_003931.3(WASF1):c.1382C>T (p.Thr461Ile)	WASF1 (T461I)	Single nucleotide variant (missense variant)	WASF1-related condition +1 more	GLikely benign
Select item 1299046	NM_003931.3(WASF1):c.1197A>G (p.Pro399=)	WASF1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656839	NM_003931.3(WASF1):c.1119T>G (p.Ala373=)	WASF1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656840	NM_003931.3(WASF1):c.776A>G (p.Gln259Arg)	WASF1 (Q259R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2579006	NM_003931.3(WASF1):c.725dup (p.Tyr242Ter)	WASF1 (Y242*)	Duplication (nonsense)	not provided	GUncertain significance
Select item 2656841	NM_003931.3(WASF1):c.547A>G (p.Asn183Asp)	WASF1 (N183D)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2656842	NM_003931.3(WASF1):c.372G>A (p.Thr124=)	WASF1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2656843	NM_003931.3(WASF1):c.307A>G (p.Ser103Gly)	WASF1 (S103G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2673075	NM_003931.3(WASF1):c.151A>G (p.Ile51Val)	WASF1 (I51V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2656844	NM_003931.3(WASF1):c.-28-6C>T	WASF1	Single nucleotide variant (intron variant)	not provided	GLikely benign