List of variants in gene GAN 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: 15

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_022041.4(GAN):c.1293C>T (p.Tyr431=)	rs2608555	0.21491
NM_022041.4(GAN):c.1239C>T (p.Ile413=)	rs61740238	0.00609
NM_022041.4(GAN):c.168-48C>G	rs77078389	0.00453
NM_022041.4(GAN):c.1684C>G (p.Pro562Ala)	rs79901179	0.00388
NM_022041.4(GAN):c.1182C>T (p.Tyr394=)	rs150102659	0.00357
NM_022041.4(GAN):c.1445C>T (p.Ala482Val)	rs146576740	0.00169
NM_022041.4(GAN):c.1612+12A>G	rs150344737	0.00135
NM_022041.4(GAN):c.1162C>T (p.Leu388=)	rs73589395	0.00103
NM_022041.4(GAN):c.358C>T (p.Leu120=)	rs113655220	0.00044
NM_022041.4(GAN):c.973+6G>A	rs372665411	0.00044
NM_022041.4(GAN):c.283-14T>C	rs369700456	0.00019
NM_022041.4(GAN):c.1086+9C>G	rs762904814	0.00001
NM_022041.4(GAN):c.1287C>G (p.Gly429=)	rs563049431
NM_022041.4(GAN):c.1314A>G (p.Val438=)
NM_022041.4(GAN):c.1428C>T (p.Val476=)

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.