List of variants in gene AGXT reported as benign for not specified

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: 17

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000030.3(AGXT):c.1020A>G (p.Ile340Met)	rs4426527	0.15412
NM_000030.3(AGXT):c.264C>T (p.Ala88=)	rs35698882	0.15328
NM_000030.3(AGXT):c.680+17C>T	rs11693280	0.14843
NM_000030.3(AGXT):c.358+13C>T	rs34995778	0.14826
NM_000030.3(AGXT):c.654G>A (p.Ser218=)	rs33958047	0.12652
NM_000030.3(AGXT):c.65A>G (p.Asn22Ser)	rs34885252	0.02454
NM_000030.3(AGXT):c.26C>A (p.Thr9Asn)	rs115014558	0.00719
NM_000030.3(AGXT):c.166-14C>T	rs180177176	0.00486
NM_000030.3(AGXT):c.976G>A (p.Val326Ile)	rs115057148	0.00394
NM_000030.3(AGXT):c.732C>A (p.Ile244=)	rs147106773	0.00234
NM_000030.3(AGXT):c.590G>A (p.Arg197Gln)	rs34664134	0.00233
NM_000030.3(AGXT):c.557C>T (p.Ala186Val)	rs117195882	0.00231
NM_000030.3(AGXT):c.836T>C (p.Ile279Thr)	rs140992177	0.00171
NM_000030.3(AGXT):c.145A>C (p.Met49Leu)	rs74205173	0.00022
NM_000030.2(AGXT):c.166-48_166-47ins74
NM_000030.3(AGXT):c.165+16A>G	rs66494441
NM_000030.3(AGXT):c.32C>T (p.Pro11Leu)	rs34116584

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.