"CAMK2G-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3053058	NM_001367534.1(CAMK2G):c.1458C>T (p.Gly486=)	CAMK2G	Single nucleotide variant (synonymous variant +2 more)	CAMK2G-related condition	GBenign
Select item 2360142	NM_001367534.1(CAMK2G):c.1409C>A (p.Ala470Asp)	CAMK2G (A377D +25 more)	Single nucleotide variant (missense variant +2 more)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3029340	NM_001367534.1(CAMK2G):c.1210G>T (p.Glu404Ter)	CAMK2G (E127* +16 more)	Single nucleotide variant (nonsense +1 more)	CAMK2G-related condition	GUncertain significance
Select item 2640594	NM_001367534.1(CAMK2G):c.1038G>A (p.Ser346=)	CAMK2G	Single nucleotide variant (synonymous variant +1 more)	CAMK2G-related condition +1 more	GLikely benign
Select item 3034327	NM_001367534.1(CAMK2G):c.918G>A (p.Thr306=)	CAMK2G	Single nucleotide variant (synonymous variant +1 more)	CAMK2G-related condition	GLikely benign
Select item 3057701	NM_001367534.1(CAMK2G):c.903+9C>T	CAMK2G	Single nucleotide variant (intron variant)	CAMK2G-related condition	GLikely benign
Select item 3052207	NM_001367534.1(CAMK2G):c.810G>A (p.Pro270=)	CAMK2G	Single nucleotide variant (synonymous variant +1 more)	CAMK2G-related condition	GLikely benign
Select item 3045737	NM_001367534.1(CAMK2G):c.141C>G (p.Thr47=)	CAMK2G	Single nucleotide variant (synonymous variant +2 more)	CAMK2G-related condition	GLikely benign
Select item 3043719	NM_001367534.1(CAMK2G):c.15C>T (p.Ala5=)	CAMK2G	Single nucleotide variant (synonymous variant +2 more)	CAMK2G-related condition	GBenign