List of variants in gene KCNA1 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000217.3(KCNA1):c.1440T>A (p.Thr480=)	rs4766309	0.75219
NM_000217.3(KCNA1):c.804G>C (p.Thr268=)	rs2227910	0.50318
NM_000217.3(KCNA1):c.684T>C (p.Cys228=)	rs1048500	0.46819
NM_000217.3(KCNA1):c.*9G>A	rs4766310	0.45248
NM_000217.3(KCNA1):c.1296C>G (p.Ser432=)	rs76066681	0.00299
NM_000217.3(KCNA1):c.237G>A (p.Glu79=)	rs149110871	0.00280
NM_000217.3(KCNA1):c.1327C>G (p.Arg443Gly)	rs150849316	0.00078
NM_000217.3(KCNA1):c.393G>A (p.Arg131=)	rs142184899	0.00039
NM_000217.3(KCNA1):c.1125C>T (p.Tyr375=)	rs144351014	0.00038
NM_000217.3(KCNA1):c.432G>C (p.Leu144=)	rs368749626	0.00003
NM_000217.3(KCNA1):c.76C>T (p.Arg26Trp)	rs373645838	0.00001
NM_000217.3(KCNA1):c.496G>C (p.Ala166Pro)	rs1179635654
NM_000217.3(KCNA1):c.607C>T (p.His203Tyr)
NM_000217.3(KCNA1):c.705G>A (p.Glu235=)	rs1555085734

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