List of variants in gene SLC39A14 reported by GeneReviews

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001128431.4(SLC39A14):c.1147G>A (p.Gly383Arg)	rs879253766
NM_001128431.4(SLC39A14):c.1407C>G (p.Asn469Lys)	rs750281602
NM_001128431.4(SLC39A14):c.292T>G (p.Phe98Val)	rs879253763
NM_001128431.4(SLC39A14):c.313G>T (p.Glu105Ter)	rs879253764
NM_001128431.4(SLC39A14):c.367C>T (p.Gln123Ter)	rs1554519011
NM_001128431.4(SLC39A14):c.751-9C>G	rs1039778197
NM_015359.6(SLC39A14):c.477_478del (p.Ser160fs)	rs879253765
NM_015359.6(SLC39A14):c.512G>A (p.Gly171Glu)	rs1554519303

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