List of variants in gene GAN reported as uncertain significance for not provided

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: 34

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HGVS	dbSNP	gnomAD frequency
NM_022041.4(GAN):c.1445C>T (p.Ala482Val)	rs146576740	0.00169
NM_022041.4(GAN):c.1162C>T (p.Leu388=)	rs73589395	0.00103
NM_022041.4(GAN):c.355A>T (p.Thr119Ser)	rs141396595	0.00086
NM_022041.4(GAN):c.730A>G (p.Ile244Val)	rs200749953	0.00051
NM_022041.4(GAN):c.670T>G (p.Ser224Ala)	rs139055455	0.00022
NM_022041.4(GAN):c.1630G>A (p.Val544Met)	rs200071978	0.00010
NM_022041.4(GAN):c.1199C>G (p.Thr400Ser)	rs368571975	0.00009
NM_022041.4(GAN):c.1148A>T (p.Asp383Val)	rs768562044	0.00004
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.972A>T (p.Ala324=)	rs1430569033	0.00003
NM_022041.4(GAN):c.1132A>G (p.Ile378Val)	rs571347913	0.00002
NM_022041.4(GAN):c.1171A>G (p.Met391Val)	rs367600164	0.00002
NM_022041.4(GAN):c.1678C>T (p.Leu560Phe)	rs143179676	0.00002
NM_022041.4(GAN):c.1241G>A (p.Gly414Asp)	rs761827117	0.00001
NM_022041.4(GAN):c.1391G>A (p.Cys464Tyr)	rs777535272	0.00001
NM_022041.4(GAN):c.1628A>G (p.Tyr543Cys)	rs879253958	0.00001
NM_022041.4(GAN):c.236C>T (p.Ser79Leu)	rs1310137430	0.00001
NM_022041.4(GAN):c.725G>A (p.Arg242Gln)	rs371906996	0.00001
GRCh37/hg19 16q23.2(chr16:81372725-81460969)x1
NM_022041.4(GAN):c.1139G>T (p.Gly380Val)	rs1427637335
NM_022041.4(GAN):c.1259A>C (p.Lys420Thr)	rs879254174
NM_022041.4(GAN):c.1315G>A (p.Glu439Lys)	rs2150691652
NM_022041.4(GAN):c.1327C>G (p.Pro443Ala)	rs150043237
NM_022041.4(GAN):c.1381G>A (p.Ala461Thr)	rs766155831
NM_022041.4(GAN):c.1583G>T (p.Ser528Ile)	rs1904284730
NM_022041.4(GAN):c.302C>A (p.Thr101Lys)	rs769446654
NM_022041.4(GAN):c.421G>T (p.Ala141Ser)	rs1057524254
NM_022041.4(GAN):c.500C>G (p.Thr167Arg)
NM_022041.4(GAN):c.565G>T (p.Val189Phe)	rs766484755
NM_022041.4(GAN):c.679G>T (p.Asp227Tyr)	rs1265208461
NM_022041.4(GAN):c.681C>G (p.Asp227Glu)	rs1910501900
NM_022041.4(GAN):c.776G>C (p.Gly259Ala)
NM_022041.4(GAN):c.998_1006del (p.Gly333_Asp335del)	rs1597405722

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