List of variants in gene KCND3 reported as benign for autosomal dominant cerebellar ataxia

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 24

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HGVS	dbSNP	gnomAD frequency
NM_001378969.1(KCND3):c.1269+15C>A	rs3738298	0.16477
NM_001378969.1(KCND3):c.264C>T (p.Pro88=)	rs17221819	0.08351
NM_001378969.1(KCND3):c.669G>C (p.Ser223=)	rs17215423	0.01872
NM_001378969.1(KCND3):c.375G>A (p.Pro125=)	rs2289723	0.01862
NM_001378969.1(KCND3):c.1323C>T (p.Tyr441=)	rs17215458	0.01243
NM_001378969.1(KCND3):c.1519-4G>T	rs72548732	0.01109
NM_001378969.1(KCND3):c.957C>G (p.Ser319=)	rs61733426	0.00386
NM_001378969.1(KCND3):c.627G>C (p.Thr209=)	rs149299911	0.00182
NM_001378969.1(KCND3):c.117T>C (p.Asp39=)	rs12720446	0.00128
NM_001378969.1(KCND3):c.1131G>T (p.Thr377=)	rs148428571	0.00038
NM_001378969.1(KCND3):c.1890G>A (p.Arg630=)	rs147262533	0.00036
NM_001378969.1(KCND3):c.870G>T (p.Arg290=)	rs200894990	0.00021
NM_001378969.1(KCND3):c.789C>T (p.Asp263=)	rs373264592	0.00019
NM_001378969.1(KCND3):c.459G>A (p.Ser153=)	rs755206508	0.00018
NM_001378969.1(KCND3):c.1354G>A (p.Glu452Lys)	rs200532657	0.00012
NM_001378969.1(KCND3):c.1269+13C>T	rs72548726	0.00009
NM_001378969.1(KCND3):c.1308C>G (p.Gly436=)	rs190703406	0.00005
NM_001378969.1(KCND3):c.624C>T (p.Gly208=)	rs772815178	0.00001
NM_001378969.1(KCND3):c.786C>T (p.Ile262=)	rs369172530	0.00001
NM_001378969.1(KCND3):c.1106+15G>A
NM_001378969.1(KCND3):c.1107-47915C>T	rs1318670
NM_001378969.1(KCND3):c.1372-6dup	rs769051410
NM_001378969.1(KCND3):c.1518+12del
NM_001378969.1(KCND3):c.633G>T (p.Pro211=)	rs35131566

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