Related gene-specific medical variations for Gene (Select 4968) - ClinVar

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Links from Gene

Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3136771	NM_003656.5(CAMK1):c.827T>C (p.Ile276Thr)	CAMK1, OGG1 (I276T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3136770	NM_003656.5(CAMK1):c.274T>C (p.Tyr92His)	CAMK1, OGG1 (Y92H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3136769	NM_003656.5(CAMK1):c.116A>G (p.Asp39Gly)	CAMK1, OGG1 (I266T +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3049965	NM_003656.5(CAMK1):c.84-45G>A	CAMK1, OGG1 (L292F +1 more)	Single nucleotide variant (synonymous variant +3 more)	OGG1-related condition	GLikely benign
Select item 2689639	NM_002542.6(OGG1):c.446A>G (p.Asn149Ser)	OGG1 (N149S)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2653502	NM_003656.5(CAMK1):c.95C>T (p.Ser32Leu)	CAMK1, OGG1 (E290K +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2653501	NM_003656.5(CAMK1):c.234T>C (p.Ile78=)	OGG1, CAMK1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2622713	NM_003656.5(CAMK1):c.417C>G (p.His139Gln)	CAMK1, OGG1 (H139Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2621039	NM_003656.5(CAMK1):c.256G>A (p.Glu86Lys)	CAMK1, OGG1 (E86K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2620688	NM_003656.5(CAMK1):c.451A>G (p.Ser151Gly)	CAMK1, OGG1 (S151G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2512428	NM_006354.5(TADA3):c.1130G>A (p.Arg377Gln)	OGG1, TADA3 (R377Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2484303	NM_003656.5(CAMK1):c.683A>C (p.Glu228Ala)	CAMK1, OGG1 (E228A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2480764	NM_003656.5(CAMK1):c.946A>G (p.Met316Val)	CAMK1, OGG1 (M316V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2405031	NM_003656.5(CAMK1):c.1034C>T (p.Pro345Leu)	CAMK1, OGG1 (P345L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2395752	NM_003656.5(CAMK1):c.564A>C (p.Glu188Asp)	CAMK1, OGG1 (E188D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2350408	NM_003656.5(CAMK1):c.245A>G (p.Asp82Gly)	CAMK1, OGG1 (D82G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2340971	NM_003656.5(CAMK1):c.992C>T (p.Thr331Met)	CAMK1, OGG1 (T331M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314710	NM_003656.5(CAMK1):c.25A>G (p.Arg9Gly)	CAMK1, OGG1 (R9G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309873	NM_003656.5(CAMK1):c.356G>C (p.Ser119Thr)	CAMK1, OGG1 (S119T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2298450	NM_006354.5(TADA3):c.1157T>A (p.Met386Lys)	OGG1, TADA3 (M386K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2248404	NM_003656.5(CAMK1):c.84-168C>T	CAMK1, OGG1 (A333T +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2220142	NM_003656.5(CAMK1):c.794T>C (p.Phe265Ser)	CAMK1, OGG1 (F265S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2211918	NM_003656.5(CAMK1):c.1073C>T (p.Pro358Leu)	CAMK1, OGG1 (P358L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 522323	NM_003656.5(CAMK1):c.84-13C>T	CAMK1, OGG1 (G348E +2 more)	Single nucleotide variant (missense variant +2 more)	Nonpapillary renal cell carcinoma	GLikely benign

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Links from Gene

Items: 24