List of variants in gene GAN reported by CeGaT Center for Human Genetics Tuebingen

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_022041.4(GAN):c.*1268C>T	rs182391687	0.00845
NM_022041.4(GAN):c.1684C>G (p.Pro562Ala)	rs79901179	0.00388
NM_022041.4(GAN):c.1445C>T (p.Ala482Val)	rs146576740	0.00169
NM_022041.4(GAN):c.730A>G (p.Ile244Val)	rs200749953	0.00051
NM_022041.4(GAN):c.1323T>C (p.Tyr441=)	rs368072478	0.00011
NM_022041.4(GAN):c.672A>G (p.Ser224=)	rs143692174	0.00011
NM_022041.4(GAN):c.445G>A (p.Val149Ile)	rs369703737	0.00004
NM_022041.4(GAN):c.490G>A (p.Val164Ile)	rs778744880	0.00003
NM_022041.4(GAN):c.1518C>T (p.Asn506=)	rs886052333	0.00002
NM_022041.4(GAN):c.1416G>A (p.Val472=)	rs998119133	0.00001
NM_022041.4(GAN):c.*1659del	rs546229255
NM_022041.4(GAN):c.1479G>A (p.Glu493=)
NM_022041.4(GAN):c.302C>A (p.Thr101Lys)	rs769446654
NM_022041.4(GAN):c.334C>T (p.Leu112=)	rs1567491415
NM_022041.4(GAN):c.681C>G (p.Asp227Glu)	rs1910501900
NM_022041.4(GAN):c.906C>T (p.Asn302=)
NM_022041.4(GAN):c.998_1006del (p.Gly333_Asp335del)	rs1597405722

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