ClinVar Miner

List of variants in gene KCNT1 studied for Epilepsy, nocturnal frontal lobe, 5

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Total variants: 26
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HGVS dbSNP
NM_020822.3(KCNT1):c.111-2A>T
NM_020822.3(KCNT1):c.1193G>A (p.Arg398Gln) rs397515407
NM_020822.3(KCNT1):c.1283G>A (p.Arg428Gln)
NM_020822.3(KCNT1):c.1402-8C>T
NM_020822.3(KCNT1):c.1421G>A (p.Arg474His)
NM_020822.3(KCNT1):c.1769+6G>A
NM_020822.3(KCNT1):c.2126G>A (p.Ser709Asn)
NM_020822.3(KCNT1):c.2166_2170del (p.Pro724fs)
NM_020822.3(KCNT1):c.2323C>G (p.Pro775Ala)
NM_020822.3(KCNT1):c.2386T>C (p.Tyr796His) rs397515406
NM_020822.3(KCNT1):c.2464C>T (p.Arg822Trp)
NM_020822.3(KCNT1):c.2688G>A (p.Met896Ile) rs797044544
NM_020822.3(KCNT1):c.2728C>T (p.Arg910Trp)
NM_020822.3(KCNT1):c.2782C>T (p.Arg928Cys) rs397515405
NM_020822.3(KCNT1):c.2824C>T (p.Leu942Phe)
NM_020822.3(KCNT1):c.2896G>A (p.Ala966Thr)
NM_020822.3(KCNT1):c.3046G>T (p.Asp1016Tyr)
NM_020822.3(KCNT1):c.3059G>A (p.Arg1020His) rs373365707
NM_020822.3(KCNT1):c.3149C>T (p.Thr1050Ile)
NM_020822.3(KCNT1):c.3388G>A (p.Ala1130Thr) rs138421850
NM_020822.3(KCNT1):c.3544A>C (p.Ile1182Leu)
NM_020822.3(KCNT1):c.785G>A (p.Arg262Gln) rs1554771469
NM_020822.3(KCNT1):c.862G>A (p.Gly288Ser) rs587777264
NM_020822.3(KCNT1):c.880C>T (p.Arg294Trp)
NM_020822.3(KCNT1):c.972C>G (p.Ile324Met)
NM_020822.3(KCNT1):c.980C>T (p.Ser327Leu)

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