"Genome-Nilou Lab"[submitter] AND "SLC29A3"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 130342	NM_018344.6(SLC29A3):c.52A>G (p.Arg18Gly)	SLC29A3 (R18G)	Single nucleotide variant (missense variant +2 more)	not specified +2 more	GBenign
Select item 130340	NM_018344.6(SLC29A3):c.383+8A>G	SLC29A3	Single nucleotide variant (intron variant)	not specified +2 more	GBenign
Select item 130341	NM_018344.6(SLC29A3):c.473C>T (p.Ser158Phe)	SLC29A3 (S158F +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GBenign; drug response
Select item 130343	NM_018344.6(SLC29A3):c.714T>C (p.Thr238=)	SLC29A3	Single nucleotide variant (synonymous variant +1 more)	not specified +2 more	GBenign
Select item 130344	NM_018344.6(SLC29A3):c.715G>A (p.Val239Ile)	SLC29A3 (V239I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +2 more	GBenign
Select item 130347	NM_018344.6(SLC29A3):c.976A>G (p.Ile326Val)	SLC29A3 (I326V +1 more)	Single nucleotide variant (3 prime UTR variant +2 more)	not specified +2 more	GBenign
Select item 130337	NM_018344.6(SLC29A3):c.1008T>C (p.Gly336=)	SLC29A3	Single nucleotide variant (3 prime UTR variant +2 more)	not provided +2 more	GBenign

ClinVar