List of variants in gene SLC29A3 reported as pathogenic by OMIM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_018344.6(SLC29A3):c.347T>G (p.Met116Arg)	rs267607057	0.00008
NM_018344.6(SLC29A3):c.1309G>A (p.Gly437Arg)	rs121912584	0.00006
NM_018344.6(SLC29A3):c.1087C>T (p.Arg363Trp)	rs387907067	0.00004
NM_018344.6(SLC29A3):c.1279G>A (p.Gly427Ser)	rs121912583	0.00002
NM_018344.6(SLC29A3):c.1088G>A (p.Arg363Gln)	rs387907066	0.00001
NM_018344.6(SLC29A3):c.1157G>A (p.Arg386Gln)	rs397515429	0.00001
NM_018344.6(SLC29A3):c.300+1G>A	rs587780463	0.00001
NM_018344.6(SLC29A3):c.607T>C (p.Ser203Pro)	rs397514626	0.00001
NM_018344.6(SLC29A3):c.1045del (p.Leu349fs)	rs869025176
NM_018344.6(SLC29A3):c.1330G>T (p.Glu444Ter)	rs267607056
NM_018344.6(SLC29A3):c.1346C>G (p.Thr449Arg)	rs267607058
NM_018344.6(SLC29A3):c.243del (p.Lys81fs)	rs1589220231
NM_018344.6(SLC29A3):c.308_309del (p.Tyr102_Phe103insTer)	rs796052139
NM_018344.6(SLC29A3):c.940del (p.Tyr314fs)	rs869025177

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.