"PreventionGenetics, part of Exact Sciences"[submitter] AND "SLC39A14" - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 740837	NM_001128431.4(SLC39A14):c.24G>T (p.Pro8=)	SLC39A14	Single nucleotide variant (synonymous variant)	SLC39A14-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 2047028	NM_001128431.4(SLC39A14):c.321G>A (p.Ser107=)	SLC39A14	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 2178627	NM_001128431.4(SLC39A14):c.885C>T (p.Asp295=)	SLC39A14	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1627844	NM_001128431.4(SLC39A14):c.939+8G>C	SLC39A14	Single nucleotide variant (intron variant)	SLC39A14-related disorder +3 more	GBenign/Likely benign
Select item 1541335	NM_001128431.4(SLC39A14):c.939+10C>G	SLC39A14	Single nucleotide variant (intron variant)	SLC39A14-related disorder +1 more	GBenign/Likely benign
Select item 758993	NM_001128431.4(SLC39A14):c.999C>T (p.Ile333=)	SLC39A14	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign

ClinVar