CSNK1G3[gene] and "single gene"[properties] - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3078289	NM_001364140.2(CSNK1G3):c.17A>G (p.Lys6Arg)	CSNK1G3 (K6R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3269890	NM_001364140.2(CSNK1G3):c.134T>C (p.Val45Ala)	CSNK1G3 (V45A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2620217	NM_001364140.2(CSNK1G3):c.193A>T (p.Thr65Ser)	CSNK1G3 (T65S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3078290	NM_001364140.2(CSNK1G3):c.305T>C (p.Val102Ala)	CSNK1G3 (V127A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2290764	NM_001364140.2(CSNK1G3):c.335A>G (p.Asn112Ser)	CSNK1G3 (N112S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2401568	NM_001364140.2(CSNK1G3):c.398C>T (p.Thr133Ile)	CSNK1G3 (T158I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3269889	NM_001364140.2(CSNK1G3):c.446G>A (p.Arg149His)	CSNK1G3 (R174H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3269891	NM_001364140.2(CSNK1G3):c.582T>A (p.Asp194Glu)	CSNK1G3 (D194E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256278	NM_001364140.2(CSNK1G3):c.584C>T (p.Pro195Leu)	CSNK1G3 (P120L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343750	NM_001364140.2(CSNK1G3):c.805C>T (p.Arg269Trp)	CSNK1G3 (R294W +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3269892	NM_001364140.2(CSNK1G3):c.907G>C (p.Asp303His)	CSNK1G3 (D190H +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388492	NM_001364140.2(CSNK1G3):c.940G>A (p.Asp314Asn)	CSNK1G3 (D238N +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208533	NM_001364140.2(CSNK1G3):c.1010C>G (p.Ala337Gly)	CSNK1G3 (A262G +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338967	NM_001364140.2(CSNK1G3):c.1049C>G (p.Ala350Gly)	CSNK1G3 (A236G +6 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3050578	NM_001364140.2(CSNK1G3):c.1179G>A (p.Ser393=)	CSNK1G3	Single nucleotide variant (synonymous variant +1 more)	CSNK1G3-related disorder	GLikely benign
Select item 3039053	NM_001364140.2(CSNK1G3):c.1186-6A>G	CSNK1G3	Single nucleotide variant (intron variant)	CSNK1G3-related disorder	GBenign
Select item 3051962	NM_001364140.2(CSNK1G3):c.1186-4A>G	CSNK1G3	Single nucleotide variant (intron variant)	CSNK1G3-related disorder	GLikely benign
Select item 2493257	NM_001364140.2(CSNK1G3):c.1186G>T (p.Val396Phe)	CSNK1G3 (V288F +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256416	NM_001364140.2(CSNK1G3):c.1196C>T (p.Ser399Phe)	CSNK1G3 (S254F +10 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3048750	NM_001364140.2(CSNK1G3):c.1353C>T (p.Thr451=)	CSNK1G3	Single nucleotide variant (synonymous variant)	CSNK1G3-related disorder	GLikely benign
Select item 3062817	GRCh37/hg19 5q23.2(chr5:122826598-123301749)x3	CSNK1G3	Copy number gain	not specified	GUncertain significance
Select item 1340486	GRCh37/hg19 5q23.2(chr5:122948549-123506769)x3	CSNK1G3	Copy number gain	not provided	GUncertain significance
Select item 687592	GRCh37/hg19 5q23.2(chr5:122882308-122947891)x1	CSNK1G3	Copy number loss	not provided	GUncertain significance

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Items: 23