List of variants in gene GAN studied 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
		ClinVar version:

Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_022041.4(GAN):c.1293C>T (p.Tyr431=)	rs2608555	0.21090
NM_022041.4(GAN):c.1086+71C>T	rs12448327	0.18756
NM_022041.4(GAN):c.1612+13C>G	rs80326128	0.00917
NM_022041.4(GAN):c.168-48C>G	rs77078389	0.00604
NM_022041.4(GAN):c.1239C>T (p.Ile413=)	rs61740238	0.00561
NM_022041.4(GAN):c.1445C>T (p.Ala482Val)	rs146576740	0.00164
NM_022041.4(GAN):c.1612+12A>G	rs150344737	0.00131
NM_022041.4(GAN):c.633+19A>G	rs112194888	0.00129
NM_022041.4(GAN):c.283-20T>C	rs371984923	0.00093
NM_022041.4(GAN):c.973+6G>A	rs372665411	0.00040
NM_022041.4(GAN):c.237G>A (p.Ser79=)	rs144007114	0.00022
NM_022041.4(GAN):c.283-14T>C	rs369700456	0.00019
NM_022041.4(GAN):c.634-15T>C	rs367608270	0.00011
NM_022041.4(GAN):c.1086+9C>G	rs762904814	0.00001
NM_022041.4(GAN):c.660T>C (p.Ala220=)	rs1555511259	0.00001
NM_022041.4(GAN):c.851+1G>A	rs747291494	0.00001
NM_022041.4(GAN):c.896A>G (p.Tyr299Cys)	rs1254823893	0.00001
GRCh37/hg19 16q23.2(chr16:81375314-81433415)
NM_022041.4(GAN):c.1287C>G (p.Gly429=)	rs563049431
NM_022041.4(GAN):c.1308G>A (p.Glu436=)
NM_022041.4(GAN):c.1338_1339delinsAA (p.Gln447Lys)	rs2507749836
NM_022041.4(GAN):c.1362A>G (p.Leu454=)	rs1057521345
NM_022041.4(GAN):c.1459A>G (p.Met487Val)
NM_022041.4(GAN):c.1593T>A (p.Val531=)	rs141592516
NM_022041.4(GAN):c.322G>A (p.Ala108Thr)	rs771660619
NM_022041.4(GAN):c.852-13T>C	rs758517277

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