"Ambry Genetics"[submitter] AND "SLC39A12"[gene] - ClinVar

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Items: 33

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2410857	NM_001145195.2(SLC39A12):c.10C>T (p.Arg4Trp)	SLC39A12 (R4W)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3164657	NM_001145195.2(SLC39A12):c.46C>G (p.Leu16Val)	SLC39A12 (L16V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3319748	NM_001145195.2(SLC39A12):c.79G>T (p.Asp27Tyr)	SLC39A12 (D27Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2269383	NM_001145195.2(SLC39A12):c.128C>T (p.Pro43Leu)	SLC39A12 (P43L)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3164651	NM_001145195.2(SLC39A12):c.139C>A (p.Leu47Ile)	SLC39A12 (L47I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2370915	NM_001145195.2(SLC39A12):c.166C>T (p.Pro56Ser)	SLC39A12 (P56S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2265040	NM_001145195.2(SLC39A12):c.195C>G (p.Ile65Met)	SLC39A12 (I65M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2346671	NM_001145195.2(SLC39A12):c.257A>G (p.Asn86Ser)	SLC39A12 (N86S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2484694	NM_001145195.2(SLC39A12):c.364A>G (p.Ile122Val)	SLC39A12 (I122V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2472653	NM_001145195.2(SLC39A12):c.373C>G (p.Gln125Glu)	SLC39A12 (Q125E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3164656	NM_001145195.2(SLC39A12):c.379G>C (p.Glu127Gln)	SLC39A12 (E127Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2601945	NM_001145195.2(SLC39A12):c.394A>G (p.Lys132Glu)	SLC39A12 (K132E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2473527	NM_001145195.2(SLC39A12):c.569A>G (p.Lys190Arg)	SLC39A12 (K190R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164658	NM_001145195.2(SLC39A12):c.609T>A (p.Ser203Arg)	SLC39A12 (S203R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305370	NM_001145195.2(SLC39A12):c.671A>C (p.Gln224Pro)	SLC39A12 (Q90P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367930	NM_001145195.2(SLC39A12):c.697T>C (p.Phe233Leu)	SLC39A12 (F99L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164659	NM_001145195.2(SLC39A12):c.719C>T (p.Ser240Phe)	SLC39A12 (S106F +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2508294	NM_001145195.2(SLC39A12):c.763C>G (p.Leu255Val)	SLC39A12 (L255V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3319747	NM_001145195.2(SLC39A12):c.857A>T (p.Gln286Leu)	SLC39A12 (Q286L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164660	NM_001145195.2(SLC39A12):c.881C>T (p.Ser294Phe)	SLC39A12 (S294F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164649	NM_001145195.2(SLC39A12):c.1018A>G (p.Ile340Val)	LOC126860872, SLC39A12 (I340V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612198	NM_001145195.2(SLC39A12):c.1097A>C (p.Lys366Thr)	SLC39A12 (K366T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215126	NM_001145195.2(SLC39A12):c.1108A>G (p.Ser370Gly)	SLC39A12 (S236G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539839	NM_001145195.2(SLC39A12):c.1141T>C (p.Ser381Pro)	SLC39A12 (S381P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513178	NM_001145195.2(SLC39A12):c.1225G>A (p.Val409Ile)	SLC39A12 (V275I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2301200	NM_001145195.2(SLC39A12):c.1319A>G (p.Glu440Gly)	SLC39A12 (E440G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278432	NM_001145195.2(SLC39A12):c.1327G>C (p.Gly443Arg)	SLC39A12 (G443R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510381	NM_001145195.2(SLC39A12):c.1364T>A (p.Ile455Asn)	SLC39A12 (I321N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341308	NM_001145195.2(SLC39A12):c.1380G>C (p.Leu460Phe)	SLC39A12 (L326F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365937	NM_001145195.2(SLC39A12):c.1417G>C (p.Asp473His)	SLC39A12 (D339H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164652	NM_001145195.2(SLC39A12):c.1570A>G (p.Ile524Val)	SLC39A12 (I390V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324234	NM_001145195.2(SLC39A12):c.1613G>T (p.Ser538Ile)	SLC39A12 (S537I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164653	NM_001145195.2(SLC39A12):c.1727C>A (p.Ala576Asp)	SLC39A12 (A576D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 33