"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "SLC30A10"[ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 295582	NM_018713.3(SLC30A10):c.1449G>A (p.Thr483=)	SLC30A10	Single nucleotide variant (synonymous variant +1 more)	Hypermanganesemia with dystonia, polycythemia, and cirrhosis +1 more	GConflicting classifications of pathogenicity
Select item 1664487	NM_018713.3(SLC30A10):c.1326T>C (p.Ser442=)	SLC30A10	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2170334	NM_018713.3(SLC30A10):c.1164G>A (p.Lys388=)	SLC30A10	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 1711238	NM_018713.3(SLC30A10):c.1089C>A (p.Ser363Arg)	SLC30A10 (S300R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 875814	NM_018713.3(SLC30A10):c.789T>C (p.Tyr263=)	SLC30A10	Single nucleotide variant (synonymous variant +1 more)	Hypermanganesemia with dystonia, polycythemia, and cirrhosis +1 more	GConflicting classifications of pathogenicity
Select item 1176222	NM_018713.3(SLC30A10):c.703G>A (p.Ala235Thr)	SLC30A10 (A172T +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2582870	NM_001376929.1(SLC30A10):c.438A>T (p.Gly146=)	SLC30A10	Single nucleotide variant (synonymous variant)	not provided	GUncertain significance

ClinVar