List of variants in gene AGXT reported by PreventionGenetics, part of Exact Sciences

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: 27

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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.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.836T>C (p.Ile279Thr)	rs140992177	0.00171
NM_000030.3(AGXT):c.508G>A (p.Gly170Arg)	rs121908529	0.00067
NM_000030.3(AGXT):c.489G>A (p.Leu163=)	rs147601535	0.00019
NM_000030.3(AGXT):c.567C>T (p.Gly189=)	rs373612587	0.00008
NM_000030.3(AGXT):c.731T>C (p.Ile244Thr)	rs121908525	0.00006
NM_000030.3(AGXT):c.795C>T (p.Pro265=)	rs760015739	0.00004
NM_000030.3(AGXT):c.507C>T (p.Phe169=)	rs1452888199	0.00001
NM_000030.3(AGXT):c.596-10C>T	rs890462970	0.00001
NM_000030.3(AGXT):c.660C>T (p.Ile220=)	rs780078312	0.00001
NM_000030.2(AGXT):c.166-48_166-47ins74
NM_000030.3(AGXT):c.-6C>T
NM_000030.3(AGXT):c.1065G>A (p.Thr355=)	rs143488099
NM_000030.3(AGXT):c.165+16A>G	rs66494441
NM_000030.3(AGXT):c.32C>A (p.Pro11His)	rs34116584
NM_000030.3(AGXT):c.32C>T (p.Pro11Leu)	rs34116584
NM_000030.3(AGXT):c.33del (p.Lys12fs)	rs180177201
NM_000030.3(AGXT):c.33dup (p.Lys12fs)	rs180177201
NM_000030.3(AGXT):c.776+3del
NM_000030.3(AGXT):c.839C>T (p.Ala280Val)	rs73106685

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