"Ambry Genetics"[submitter] AND "MAGEA6"[gene] - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2484485	NM_005363.5(MAGEA6):c.916G>A (p.Glu306Lys)	MAGEA6 (E306K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546209	NM_005363.5(MAGEA6):c.884G>A (p.Gly295Glu)	MAGEA6 (G295E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122085	NM_005363.5(MAGEA6):c.877A>C (p.Ile293Leu)	MAGEA6 (I293L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612242	NM_005363.5(MAGEA6):c.864C>G (p.His288Gln)	MAGEA6 (H288Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208718	NM_005363.5(MAGEA6):c.850G>A (p.Val284Met)	MAGEA6 (V284M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122084	NM_005363.5(MAGEA6):c.813C>G (p.Phe271Leu)	MAGEA6 (F271L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360602	NM_005363.5(MAGEA6):c.751G>A (p.Val251Met)	MAGEA6 (V251M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367566	NM_005363.5(MAGEA6):c.717C>G (p.Phe239Leu)	MAGEA6 (F239L)	Single nucleotide variant (no sequence alteration +1 more)	not specified	GLikely benign
Select item 3122083	NM_005363.5(MAGEA6):c.683T>C (p.Leu228Ser)	MAGEA6 (L228S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122082	NM_005363.5(MAGEA6):c.550C>G (p.Leu184Val)	MAGEA6 (L184V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122081	NM_005363.5(MAGEA6):c.521A>T (p.His174Leu)	MAGEA6 (H174L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3122080	NM_005363.5(MAGEA6):c.467A>G (p.Asp156Gly)	MAGEA6 (D156G)	Single nucleotide variant (no sequence alteration +1 more)	not specified	GUncertain significance
Select item 2387412	NM_005362.4(MAGEA3):c.418G>A (p.Val140Ile)	MAGEA6 (V140I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481656	NM_005363.5(MAGEA6):c.403A>G (p.Met135Val)	MAGEA6 (M135V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476467	NM_005363.5(MAGEA6):c.355T>C (p.Phe119Leu)	MAGEA6 (F119L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235066	NM_005363.5(MAGEA6):c.325C>T (p.Leu109Phe)	MAGEA6 (L109F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535818	NM_005363.5(MAGEA6):c.323C>G (p.Ala108Gly)	MAGEA6 (A108G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318063	NM_005363.5(MAGEA6):c.258C>A (p.Asp86Glu)	MAGEA6 (D86E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519926	NM_005363.5(MAGEA6):c.248C>T (p.Ser83Phe)	MAGEA6 (S83F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495993	NM_005363.5(MAGEA6):c.233C>G (p.Pro78Arg)	MAGEA6 (P78R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232543	NM_005363.5(MAGEA6):c.172T>G (p.Ser58Ala)	MAGEA6 (S58A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303963	NM_005363.5(MAGEA6):c.169G>A (p.Glu57Lys)	MAGEA6 (E57K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2232542	NM_005363.5(MAGEA6):c.160C>A (p.Pro54Thr)	MAGEA6 (P54T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 23