"Ambry Genetics"[submitter] AND "SLC39A11"[gene] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2593375	NM_139177.4(SLC39A11):c.994G>A (p.Val332Ile)	SLC39A11 (V332I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206739	NM_139177.4(SLC39A11):c.892G>A (p.Val298Met)	SLC39A11 (V305M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2227215	NM_139177.4(SLC39A11):c.727C>A (p.Leu243Ile)	SLC39A11 (L243I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164648	NM_139177.4(SLC39A11):c.644C>T (p.Thr215Met)	SLC39A11 (T215M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292515	NM_139177.4(SLC39A11):c.592A>G (p.Asn198Asp)	SLC39A11 (N198D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164647	NM_139177.4(SLC39A11):c.584C>T (p.Thr195Ile)	SLC39A11 (T195I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217420	NM_139177.4(SLC39A11):c.557G>A (p.Arg186Lys)	SLC39A11 (R193K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401348	NM_139177.4(SLC39A11):c.552G>C (p.Trp184Cys)	SLC39A11 (W184C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164646	NM_139177.4(SLC39A11):c.542G>A (p.Gly181Asp)	SLC39A11 (G181D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164645	NM_139177.4(SLC39A11):c.497C>T (p.Pro166Leu)	SLC39A11 (P166L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334380	NM_139177.4(SLC39A11):c.493G>A (p.Gly165Ser)	SLC39A11 (G165S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164643	NM_139177.4(SLC39A11):c.430+6G>A	LOC126862633, SLC39A11 (A146T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2323113	NM_139177.4(SLC39A11):c.406G>A (p.Glu136Lys)	LOC126862633, SLC39A11 (E136K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164642	NM_139177.4(SLC39A11):c.389C>T (p.Pro130Leu)	LOC126862633, SLC39A11 (P130L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553623	NM_139177.4(SLC39A11):c.301C>G (p.His101Asp)	SLC39A11 (H101D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2546633	NM_139177.4(SLC39A11):c.289C>T (p.Leu97Phe)	SLC39A11 (L97F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539378	NM_139177.4(SLC39A11):c.260T>C (p.Leu87Pro)	SLC39A11 (L87P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349271	NM_139177.4(SLC39A11):c.256A>G (p.Thr86Ala)	SLC39A11 (T86A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372988	NM_139177.4(SLC39A11):c.237C>G (p.Phe79Leu)	SLC39A11 (F79L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164641	NM_139177.4(SLC39A11):c.199G>T (p.Ala67Ser)	SLC39A11 (A67S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2492527	NM_139177.4(SLC39A11):c.153G>A (p.Met51Ile)	SLC39A11 (M51I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478606	NM_139177.4(SLC39A11):c.122A>G (p.Asp41Gly)	SLC39A11 (D41G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164640	NM_139177.4(SLC39A11):c.106C>G (p.Gln36Glu)	SLC39A11 (Q36E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377796	NM_139177.4(SLC39A11):c.91G>A (p.Val31Ile)	SLC39A11 (V31I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2548210	NM_139177.4(SLC39A11):c.44C>A (p.Thr15Asn)	SLC39A11 (T15N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 25