"Fulgent Genetics, Fulgent Genetics"[submitter] AND "SLC39A4"[gene] - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 985707	NM_130849.4(SLC39A4):c.1465_1474+4del	SLC39A4	Deletion (splice donor variant)	not provided +3 more	GPathogenic/Likely pathogenic
Select item 751322	NM_130849.4(SLC39A4):c.1299C>T (p.Asp433=)	SLC39A4	Single nucleotide variant (synonymous variant)	Hereditary acrodermatitis enteropathica +1 more	GLikely benign
Select item 362242	NM_130849.4(SLC39A4):c.1069A>G (p.Thr357Ala)	SLC39A4 (T357A +2 more)	Single nucleotide variant (missense variant)	Hereditary acrodermatitis enteropathica +2 more	GBenign
Select item 1484281	NM_130849.4(SLC39A4):c.977-1G>A	SLC39A4	Single nucleotide variant (splice acceptor variant)	Hereditary acrodermatitis enteropathica +1 more	GLikely pathogenic
Select item 362245	NM_130849.4(SLC39A4):c.948C>T (p.Pro316=)	SLC39A4	Single nucleotide variant (synonymous variant)	Hereditary acrodermatitis enteropathica +1 more	GBenign/Likely benign
Select item 1456654	NM_130849.4(SLC39A4):c.862del (p.Gly287_Val288insTer)	SLC39A4	Deletion (nonsense)	Hereditary acrodermatitis enteropathica +1 more	GPathogenic/Likely pathogenic
Select item 1204083	NM_130849.4(SLC39A4):c.659C>T (p.Thr220Met)	SLC39A4 (T126M +2 more)	Single nucleotide variant (missense variant)	Hereditary acrodermatitis enteropathica +2 more	GUncertain significance
Select item 3537	NM_130849.4(SLC39A4):c.599C>T (p.Pro200Leu)	SLC39A4 (P200L +1 more)	Single nucleotide variant (missense variant)	SLC39A4-related disorder +2 more	GPathogenic/Likely pathogenic
Select item 1481691	NM_130849.4(SLC39A4):c.475-2A>G	SLC39A4	Single nucleotide variant (splice acceptor variant)	not provided +1 more	GLikely pathogenic
Select item 741302	NM_130849.4(SLC39A4):c.297C>T (p.Ala99=)	SLC39A4	Single nucleotide variant (synonymous variant +1 more)	Hereditary acrodermatitis enteropathica +1 more	GLikely benign
Select item 362268	NM_130849.4(SLC39A4):c.-10G>A	SLC39A4	Single nucleotide variant (5 prime UTR variant)	Hereditary acrodermatitis enteropathica	GUncertain significance