"IQGAP3-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

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Items: 34

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3034682	NM_178229.5(IQGAP3):c.4563C>T (p.Pro1521=)	IQGAP3	Single nucleotide variant (synonymous variant)	IQGAP3-related condition	GLikely benign
Select item 3038988	NM_178229.5(IQGAP3):c.4383G>A (p.Gly1461=)	IQGAP3	Single nucleotide variant (synonymous variant)	IQGAP3-related condition	GLikely benign
Select item 3042046	NM_178229.5(IQGAP3):c.4334G>A (p.Arg1445His)	IQGAP3 (R1445H)	Single nucleotide variant (missense variant)	IQGAP3-related condition	GBenign
Select item 3044968	NM_178229.5(IQGAP3):c.4268G>A (p.Arg1423His)	IQGAP3 (R1423H)	Single nucleotide variant (missense variant)	IQGAP3-related condition	GLikely benign
Select item 3051289	NM_178229.5(IQGAP3):c.4248G>A (p.Pro1416=)	IQGAP3	Single nucleotide variant (synonymous variant)	IQGAP3-related condition	GLikely benign
Select item 3041639	NM_178229.5(IQGAP3):c.4122C>T (p.Ala1374=)	IQGAP3	Single nucleotide variant (synonymous variant)	IQGAP3-related condition	GBenign
Select item 3055445	NM_178229.5(IQGAP3):c.4005G>A (p.Thr1335=)	IQGAP3	Single nucleotide variant (synonymous variant)	IQGAP3-related condition	GBenign
Select item 3034800	NM_178229.5(IQGAP3):c.3987C>T (p.Ile1329=)	IQGAP3	Single nucleotide variant (synonymous variant)	IQGAP3-related condition	GLikely benign
Select item 3056368	NM_178229.5(IQGAP3):c.3976+5G>A	IQGAP3	Single nucleotide variant (intron variant)	IQGAP3-related condition	GBenign
Select item 3057904	NM_178229.5(IQGAP3):c.3873+8G>T	IQGAP3	Single nucleotide variant (intron variant)	IQGAP3-related condition	GLikely benign
Select item 3033216	NM_178229.5(IQGAP3):c.3846C>T (p.Thr1282=)	IQGAP3	Single nucleotide variant (synonymous variant)	IQGAP3-related condition	GLikely benign
Select item 3040922	NM_178229.5(IQGAP3):c.3798C>T (p.Asp1266=)	IQGAP3	Single nucleotide variant (synonymous variant)	IQGAP3-related condition	GLikely benign
Select item 3040560	NM_178229.5(IQGAP3):c.3663T>C (p.Ala1221=)	IQGAP3	Single nucleotide variant (synonymous variant)	IQGAP3-related condition	GBenign
Select item 3035396	NM_178229.5(IQGAP3):c.3564C>T (p.Asp1188=)	IQGAP3	Single nucleotide variant (synonymous variant)	IQGAP3-related condition	GLikely benign
Select item 3034730	NM_178229.5(IQGAP3):c.3507+5G>A	IQGAP3	Single nucleotide variant (intron variant)	IQGAP3-related condition	GLikely benign
Select item 3058742	NM_178229.5(IQGAP3):c.3483C>T (p.Asp1161=)	IQGAP3	Single nucleotide variant (synonymous variant)	IQGAP3-related condition	GLikely benign
Select item 3059556	NM_178229.5(IQGAP3):c.3370G>A (p.Ala1124Thr)	IQGAP3 (A1124T)	Single nucleotide variant (missense variant)	IQGAP3-related condition	GBenign
Select item 3041996	NM_178229.5(IQGAP3):c.2907C>T (p.Tyr969=)	IQGAP3	Single nucleotide variant (synonymous variant)	IQGAP3-related condition	GLikely benign
Select item 3041560	NM_178229.5(IQGAP3):c.1933G>A (p.Asp645Asn)	IQGAP3 (D645N)	Single nucleotide variant (missense variant)	IQGAP3-related condition	GBenign
Select item 775144	NM_178229.5(IQGAP3):c.1778G>T (p.Arg593Leu)	IQGAP3 (R593L)	Single nucleotide variant (missense variant)	IQGAP3-related condition +1 more	GBenign
Select item 3042418	NM_178229.5(IQGAP3):c.1289G>A (p.Gly430Glu)	IQGAP3 (G430E)	Single nucleotide variant (missense variant)	IQGAP3-related condition +1 more	GLikely benign
Select item 3052397	NM_178229.5(IQGAP3):c.1288G>C (p.Gly430Arg)	IQGAP3 (G430R)	Single nucleotide variant (missense variant)	IQGAP3-related condition	GLikely benign
Select item 3056677	NM_178229.5(IQGAP3):c.1185C>T (p.Asp395=)	IQGAP3	Single nucleotide variant (synonymous variant)	IQGAP3-related condition	GBenign
Select item 3039668	NM_178229.5(IQGAP3):c.1148G>A (p.Arg383Gln)	IQGAP3 (R383Q)	Single nucleotide variant (missense variant)	IQGAP3-related condition	GBenign
Select item 2633330	NM_178229.5(IQGAP3):c.1132C>T (p.Leu378Phe)	IQGAP3 (L378F)	Single nucleotide variant (missense variant)	IQGAP3-related condition	GUncertain significance
Select item 3057958	NM_178229.5(IQGAP3):c.1042-7C>G	IQGAP3	Single nucleotide variant (intron variant)	IQGAP3-related condition	GLikely benign
Select item 3058318	NM_178229.5(IQGAP3):c.975G>A (p.Gly325=)	IQGAP3	Single nucleotide variant (synonymous variant)	IQGAP3-related condition	GLikely benign
Select item 3039240	NM_178229.5(IQGAP3):c.792G>A (p.Arg264=)	IQGAP3	Single nucleotide variant (synonymous variant)	IQGAP3-related condition	GLikely benign
Select item 3043495	NM_178229.5(IQGAP3):c.644A>G (p.Asn215Ser)	IQGAP3 (N215S)	Single nucleotide variant (missense variant)	IQGAP3-related condition	GLikely benign
Select item 777950	NM_178229.5(IQGAP3):c.531C>A (p.Ser177=)	IQGAP3	Single nucleotide variant (synonymous variant)	IQGAP3-related condition +1 more	GBenign
Select item 3037707	NM_178229.5(IQGAP3):c.528G>A (p.Ala176=)	IQGAP3	Single nucleotide variant (synonymous variant)	IQGAP3-related condition	GLikely benign
Select item 3044170	NM_178229.5(IQGAP3):c.438-7T>C	IQGAP3	Single nucleotide variant (intron variant)	IQGAP3-related condition	GLikely benign
Select item 3033398	NM_178229.5(IQGAP3):c.258C>T (p.Tyr86=)	IQGAP3	Single nucleotide variant (synonymous variant)	IQGAP3-related condition	GLikely benign
Select item 3055968	NM_178229.5(IQGAP3):c.28T>C (p.Trp10Arg)	IQGAP3 (W10R)	Single nucleotide variant (missense variant)	IQGAP3-related condition	GBenign

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Items: 34