"PreventionGenetics, part of Exact Sciences"[submitter] AND "SRGAP3"[g - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 729518	NM_014850.4(SRGAP3):c.3241G>A (p.Val1081Met)	SRGAP3 (V1057M +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 2629106	NM_014850.4(SRGAP3):c.3070G>A (p.Ala1024Thr)	SRGAP3 (A1000T +1 more)	Single nucleotide variant (missense variant)	SRGAP3-related disorder	GUncertain significance
Select item 782421	NM_014850.4(SRGAP3):c.3036C>T (p.Pro1012=)	SRGAP3	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 708765	NM_014850.4(SRGAP3):c.2817G>A (p.Ser939=)	SRGAP3	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 729048	NM_014850.4(SRGAP3):c.2680A>G (p.Ser894Gly)	SRGAP3 (S870G +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 3048506	NM_014850.4(SRGAP3):c.2634C>A (p.Gly878=)	SRGAP3	Single nucleotide variant (synonymous variant)	SRGAP3-related disorder	GLikely benign
Select item 790643	NM_014850.4(SRGAP3):c.2535C>T (p.Tyr845=)	SRGAP3	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 714171	NM_014850.4(SRGAP3):c.2376C>T (p.Leu792=)	SRGAP3	Single nucleotide variant (synonymous variant)	SRGAP3-related disorder +1 more	GBenign
Select item 2636741	NM_014850.4(SRGAP3):c.2164G>A (p.Glu722Lys)	SRGAP3 (E698K +1 more)	Single nucleotide variant (missense variant)	SRGAP3-related disorder	GUncertain significance
Select item 732286	NM_014850.4(SRGAP3):c.2163C>T (p.Ser721=)	SRGAP3	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 773569	NM_014850.4(SRGAP3):c.1905C>T (p.Phe635=)	SRGAP3	Single nucleotide variant (synonymous variant)	SRGAP3-related disorder +1 more	GLikely benign
Select item 725709	NM_014850.4(SRGAP3):c.1882A>G (p.Ile628Val)	SRGAP3 (I604V +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 789466	NM_014850.4(SRGAP3):c.1698C>T (p.Asp566=)	SRGAP3	Single nucleotide variant (synonymous variant)	SRGAP3-related disorder +1 more	GLikely benign
Select item 775843	NM_014850.4(SRGAP3):c.1563T>G (p.Leu521=)	SRGAP3	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3056662	NM_014850.4(SRGAP3):c.1408+10C>G	SRGAP3	Single nucleotide variant (intron variant)	SRGAP3-related disorder	GBenign
Select item 3057847	NM_014850.4(SRGAP3):c.1164G>A (p.Gln388=)	SRGAP3	Single nucleotide variant (synonymous variant)	SRGAP3-related disorder	GLikely benign
Select item 775844	NM_014850.4(SRGAP3):c.975C>G (p.Val325=)	SRGAP3	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 720298	NM_014850.4(SRGAP3):c.971A>T (p.Gln324Leu)	SRGAP3 (Q324L)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 3055684	NM_014850.4(SRGAP3):c.969T>C (p.Asn323=)	SRGAP3	Single nucleotide variant (synonymous variant)	SRGAP3-related disorder	GBenign
Select item 785998	NM_014850.4(SRGAP3):c.870C>T (p.Asn290=)	SRGAP3	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3033934	NM_014850.4(SRGAP3):c.858A>T (p.Ser286=)	SRGAP3	Single nucleotide variant (synonymous variant)	SRGAP3-related disorder	GLikely benign
Select item 785999	NM_014850.4(SRGAP3):c.700C>T (p.Leu234=)	SRGAP3	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 723978	NM_014850.4(SRGAP3):c.615C>T (p.His205=)	SRGAP3	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 724506	NM_014850.4(SRGAP3):c.606G>A (p.Leu202=)	SRGAP3	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 723979	NM_014850.4(SRGAP3):c.531G>A (p.Ala177=)	SRGAP3	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 733314	NM_014850.4(SRGAP3):c.171T>G (p.Ala57=)	SRGAP3	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 783214	NM_014850.4(SRGAP3):c.51T>C (p.Tyr17=)	SRGAP3	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign

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Items: 27