"Ambry Genetics"[submitter] AND "SLC39A10"[gene] - ClinVar

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Items: 34

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2539644	NM_020342.3(SLC39A10):c.8T>C (p.Val3Ala)	SLC39A10 (V3A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164633	NM_020342.3(SLC39A10):c.27T>A (p.Phe9Leu)	SLC39A10 (F9L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332163	NM_020342.3(SLC39A10):c.208C>T (p.Arg70Cys)	SLC39A10 (R70C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246827	NM_020342.3(SLC39A10):c.307G>T (p.Asp103Tyr)	SLC39A10 (D103Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164634	NM_020342.3(SLC39A10):c.319G>A (p.Asp107Asn)	SLC39A10 (D107N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164635	NM_020342.3(SLC39A10):c.326T>C (p.Val109Ala)	SLC39A10 (V109A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164636	NM_020342.3(SLC39A10):c.341T>C (p.Ile114Thr)	SLC39A10 (I114T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3319735	NM_020342.3(SLC39A10):c.475A>G (p.Thr159Ala)	SLC39A10 (T159A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3319734	NM_020342.3(SLC39A10):c.521A>G (p.His174Arg)	SLC39A10 (H174R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164637	NM_020342.3(SLC39A10):c.530G>A (p.Arg177His)	SLC39A10 (R177H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3319739	NM_020342.3(SLC39A10):c.536G>A (p.Arg179His)	SLC39A10 (R179H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2466076	NM_020342.3(SLC39A10):c.548G>A (p.Arg183His)	SLC39A10 (R183H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2240464	NM_020342.3(SLC39A10):c.664G>A (p.Glu222Lys)	SLC39A10 (E222K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2204157	NM_020342.3(SLC39A10):c.686C>A (p.Pro229Gln)	SLC39A10 (P229Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164639	NM_020342.3(SLC39A10):c.806C>T (p.Pro269Leu)	SLC39A10 (P269L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456694	NM_020342.3(SLC39A10):c.865G>A (p.Asp289Asn)	SLC39A10 (D289N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470442	NM_020342.3(SLC39A10):c.944A>G (p.His315Arg)	SLC39A10 (H315R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340239	NM_020342.3(SLC39A10):c.959C>T (p.Ala320Val)	SLC39A10 (A320V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3319738	NM_020342.3(SLC39A10):c.1010G>A (p.Cys337Tyr)	SLC39A10 (C337Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367364	NM_020342.3(SLC39A10):c.1054A>T (p.Asn352Tyr)	SLC39A10 (N352Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3319737	NM_020342.3(SLC39A10):c.1351A>G (p.Met451Val)	SLC39A10 (M451V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3319741	NM_020342.3(SLC39A10):c.1370T>C (p.Leu457Pro)	SLC39A10 (L457P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3319736	NM_020342.3(SLC39A10):c.1733A>T (p.Asn578Ile)	SLC39A10 (N578I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526835	NM_020342.3(SLC39A10):c.1813A>G (p.Ile605Val)	SLC39A10 (I605V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164626	NM_020342.3(SLC39A10):c.1858G>T (p.Asp620Tyr)	SLC39A10 (D620Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363588	NM_020342.3(SLC39A10):c.1873G>A (p.Ala625Thr)	SLC39A10 (A625T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164627	NM_020342.3(SLC39A10):c.1891G>A (p.Glu631Lys)	SLC39A10 (E631K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316256	NM_020342.3(SLC39A10):c.2023A>T (p.Met675Leu)	SLC39A10 (M675L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164628	NM_020342.3(SLC39A10):c.2182G>A (p.Val728Ile)	SLC39A10 (V728I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164629	NM_020342.3(SLC39A10):c.2216C>T (p.Ala739Val)	SLC39A10 (A739V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164630	NM_020342.3(SLC39A10):c.2218A>G (p.Met740Val)	SLC39A10 (M740V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2473902	NM_020342.3(SLC39A10):c.2266G>A (p.Ala756Thr)	SLC39A10 (A756T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164631	NM_020342.3(SLC39A10):c.2377C>A (p.His793Asn)	SLC39A10 (H793N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337100	NM_020342.3(SLC39A10):c.2399A>G (p.Gln800Arg)	SLC39A10 (Q800R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 34