"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "CAMK2G"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2640591	NM_001367534.1(CAMK2G):c.1638G>A (p.Gln546=)	CAMK2G	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2640592	NM_001367534.1(CAMK2G):c.1439C>T (p.Thr480Met)	CAMK2G (T165M +25 more)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely benign
Select item 2640593	NM_001367534.1(CAMK2G):c.1381A>T (p.Ile461Phe)	CAMK2G (I146F +25 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 3025623	NM_001367534.1(CAMK2G):c.1135G>A (p.Ala379Thr)	CAMK2G (A117T +7 more)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely benign
Select item 1701140	NM_001367534.1(CAMK2G):c.1044_1045delinsTA (p.Gly349Ser)	CAMK2G (G106S +7 more)	Indel (missense variant +1 more)	not provided	GUncertain significance
Select item 1335041	NM_001367534.1(CAMK2G):c.1044C>T (p.Gly348=)	CAMK2G	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
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 2640595	NM_001367534.1(CAMK2G):c.26G>A (p.Arg9His)	CAMK2G, LOC130004098 (R9H)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance

ClinVar